ENST00000531452.5 RNF214
Information
- Transcript ID
- ENST00000531452.5
- Genome
- hg19
- Position
- chr11:117,103,452-117,156,404
- Strand
- +
- CDS length
- 2,112
- Amino acid length
- 704
- Gene symbol
- RNF214
- Gene type
- protein-coding
- Gene description
- ring finger protein 214
- Gene Entrez Gene ID
- 257160
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Exon
Exon number | Start | Stop |
---|---|---|
1 | 117,103,452 | 117,103,491 |
2 | 117,104,983 | 117,105,095 |
3 | 117,109,317 | 117,109,827 |
4 | 117,110,517 | 117,110,576 |
5 | 117,115,161 | 117,115,301 |
6 | 117,117,525 | 117,117,664 |
7 | 117,150,624 | 117,150,720 |
8 | 117,150,887 | 117,150,975 |
9 | 117,152,030 | 117,152,120 |
10 | 117,152,316 | 117,152,414 |
11 | 117,152,610 | 117,152,986 |
12 | 117,153,120 | 117,153,252 |
13 | 117,153,462 | 117,153,566 |
14 | 117,153,831 | 117,153,926 |
15 | 117,155,802 | 117,156,404 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
2 | CDS | 117,104,989 | 117,105,095 |
3 | CDS | 117,109,317 | 117,109,827 |
4 | CDS | 117,110,517 | 117,110,576 |
5 | CDS | 117,115,161 | 117,115,301 |
6 | CDS | 117,117,525 | 117,117,664 |
7 | CDS | 117,150,624 | 117,150,720 |
8 | CDS | 117,150,887 | 117,150,975 |
9 | CDS | 117,152,030 | 117,152,120 |
10 | CDS | 117,152,316 | 117,152,414 |
11 | CDS | 117,152,610 | 117,152,986 |
12 | CDS | 117,153,120 | 117,153,252 |
13 | CDS | 117,153,462 | 117,153,566 |
14 | CDS | 117,153,831 | 117,153,926 |
15 | CDS | 117,155,802 | 117,155,867 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr11 | 117,232,736 | 117,285,688 | Link |
CDS sequence
ATGGCAGCGTCTGAGGTTGCTGGTGTTGTGGCCAATGCCCCCAGTCCTCCGGAATCTTCTAGTTTATGTGCTTCCAAATCAGACGAAGGTCTCCCAGATGGTCTAAGCACCAAAGACTCTGCACAGAAGCAGAAGAACTCGCCTCTGTTGAGTGTAAGTAGCCAAACAATAACCAAGGAGAATAACAGAAATGTCCATTTGGAGCACTCAGAGCAGAATCCTGGTTCATCAGCAGGTGACACCTCAGCAGCGCACCAGGTGGTTTTAGGAGAAAACTTGATAGCCACAGCCCTTTGTCTTTCTGGCAGTGGGTCTCAGTCTGATTTGAAGGATGTGGCCAGCACAGCAGGAGAGGAGGGGGACACAAGCCTTCGGGAGAGCCTCCATCCAGTCACTCGGTCTCTTAAGGCAGGGTGCCATACTAAGCAGCTTGCCTCCAGGAATTGCTCTGAAGAGAAATCCCCACAAACCTCCATCCTAAAGGAAGGTAACAGGGACACAAGCTTGGATTTCCGACCTGTAGTGTCTCCAGCAAATGGGGTTGAAGGAGTCCGAGTGGATCAGGATGATGATCAAGATAGCTCTTCCCTGAAGCTTTCTCAGAACATTGCTGTACAGACTGACTTTAAGACAGCTGATTCAGAGGTAAACACAGATCAAGATATTGAAAAGAATTTGGATAAAATGATGACAGAGAGAACCCTGTTGAAAGAGCGTTACCAGGAGGTCCTGGACAAACAGAGGCAAGTGGAGAATCAGCTCCAAGTGCAATTAAAGCAGCTTCAGCAAAGGAGAGAAGAGGAAATGAAGAATCACCAGGAGATATTAAAGGCTATTCAGGATGTGACAATAAAGCGGGAAGAAACAAAGAAGAAGATAGAGAAAGAGAAGAAGGAGTTTTTGCAGAAGGAGCAGGATCTGAAAGCTGAAATTGAGAAGCTTTGTGAGAAGGGCAGAAGAGAGGTGTGGGAAATGGAACTGGATAGACTCAAGAATCAGGATGGCGAAATAAATAGGAACATTATGGAAGAGACTGAACGGGCCTGGAAGGCAGAGATCTTATCACTAGAGAGCCGGAAAGAGTTACTGGTACTGAAACTAGAAGAAGCAGAAAAAGAGGCAGAATTGCACCTTACTTACCTCAAGTCAACTCCCCCAACACTGGAGACAGTTCGTTCCAAACAGGAGTGGGAGACGAGACTGAATGGAGTTCGGATAATGAAAAAGAATGTTCGTGACCAATTTAATAGTCATATCCAGTTAGTGAGGAACGGAGCCAAGCTGAGCAGCCTTCCTCAAATCCCTACTCCCACTTTACCTCCACCCCCATCAGAGACAGACTTCATGCTTCAGGTGTTTCAACCCAGTCCCTCTCTGGCTCCTCGGATGCCCTTCTCCATTGGGCAGGTCACAATGCCCATGGTTATGCCCAGTGCAGATCCCCGCTCCTTGTCTTTCCCAATCCTGAACCCTGCCCTTTCCCAGCCCAGCCAGCCTTCCTCACCCCTTCCTGGCTCCCATGGCAGAAATAGCCCTGGCTTGGGTTCCCTTGTCAGCCCCCACGGTCCACACATGCCCCCTGCCGCCTCCATCCCACCTCCCCCAGGCTTGGGCGGTGTTAAGGCTTCTGCTGAAACTCCCCGGCCCCAACCAGTAGACAAACTGGAGAAGATCCTGGAGAAGCTGCTGACCCGGTTCCCACAGTGCAATAAGGCCCAGATGACCAACATTCTTCAGCAGATCAAGACAGCACGTACCACCATGGCAGGCCTGACCATGGAGGAACTTATCCAGTTGGTTGCTGCACGACTGGCAGAACATGAGCGGGTGGCAGCAAGTACTCAGCCACTTGGTCGCATCCGGGCCTTGTTCCCTGCTCCACTGGCCCAAATCAGTACCCCAATGTTCTTGCCTTCTGCCCAAGTTTCATATCCTGGAAGGTCTTCACATGCTCCAGCCACCTGTAAGCTATGTCTAATGTGCCAGAAACTCGTCCAGCCCAGTGAGCTGCATCCAATGGCGTGTACCCATGTATTGCACAAGGAGTGTATCAAATTCTGGGCCCAGACCAACACAAATGACACTTGTCCCTTTTGTCCAACTCTTAAATGA
Amino sequence
MAASEVAGVVANAPSPPESSSLCASKSDEGLPDGLSTKDSAQKQKNSPLLSVSSQTITKENNRNVHLEHSEQNPGSSAGDTSAAHQVVLGENLIATALCLSGSGSQSDLKDVASTAGEEGDTSLRESLHPVTRSLKAGCHTKQLASRNCSEEKSPQTSILKEGNRDTSLDFRPVVSPANGVEGVRVDQDDDQDSSSLKLSQNIAVQTDFKTADSEVNTDQDIEKNLDKMMTERTLLKERYQEVLDKQRQVENQLQVQLKQLQQRREEEMKNHQEILKAIQDVTIKREETKKKIEKEKKEFLQKEQDLKAEIEKLCEKGRREVWEMELDRLKNQDGEINRNIMEETERAWKAEILSLESRKELLVLKLEEAEKEAELHLTYLKSTPPTLETVRSKQEWETRLNGVRIMKKNVRDQFNSHIQLVRNGAKLSSLPQIPTPTLPPPPSETDFMLQVFQPSPSLAPRMPFSIGQVTMPMVMPSADPRSLSFPILNPALSQPSQPSSPLPGSHGRNSPGLGSLVSPHGPHMPPAASIPPPPGLGGVKASAETPRPQPVDKLEKILEKLLTRFPQCNKAQMTNILQQIKTARTTMAGLTMEELIQLVAARLAEHERVAASTQPLGRIRALFPAPLAQISTPMFLPSAQVSYPGRSSHAPATCKLCLMCQKLVQPSELHPMACTHVLHKECIKFWAQTNTNDTCPFCPTLK*