ENST00000064780.7 RELT
Information
- Transcript ID
- ENST00000064780.7
- Genome
- hg38
- Position
- chr11:73,376,399-73,397,474
- Strand
- +
- CDS length
- 1,293
- Amino acid length
- 431
- Gene symbol
- RELT
- Gene type
- protein-coding
- Gene description
- RELT TNF receptor
- Gene Entrez Gene ID
- 84957
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 | : |
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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 | 73,376,399 | 73,376,499 |
2 | 73,389,112 | 73,389,181 |
3 | 73,390,551 | 73,390,625 |
4 | 73,390,755 | 73,390,921 |
5 | 73,391,144 | 73,391,223 |
6 | 73,392,211 | 73,392,468 |
7 | 73,393,837 | 73,393,917 |
8 | 73,394,236 | 73,394,317 |
9 | 73,394,477 | 73,394,734 |
10 | 73,395,087 | 73,395,285 |
11 | 73,395,444 | 73,397,474 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
2 | CDS | 73,389,137 | 73,389,181 |
3 | CDS | 73,390,551 | 73,390,625 |
4 | CDS | 73,390,755 | 73,390,921 |
5 | CDS | 73,391,144 | 73,391,223 |
6 | CDS | 73,392,211 | 73,392,468 |
7 | CDS | 73,393,837 | 73,393,917 |
8 | CDS | 73,394,236 | 73,394,317 |
9 | CDS | 73,394,477 | 73,394,734 |
10 | CDS | 73,395,087 | 73,395,285 |
11 | CDS | 73,395,444 | 73,395,491 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr11 | 73,087,444 | 73,108,519 | Link |
CDS sequence
ATGAAGCCAAGTCTGCTGTGCCGGCCCCTGTCCTGCTTCCTTATGCTGCTGCCCTGGCCTCTCGCCACCCTGACATCAACAACCCTTTGGCAGTGCCCACCTGGGGAGGAGCCCGACCTGGACCCAGGGCAGGGCACATTATGCAGGCCCTGCCCCCCAGGCACCTTCTCAGCTGCATGGGGCTCCAGCCCATGCCAGCCCCATGCCCGTTGCAGCCTTTGGAGGAGGCTGGAGGCCCAGGTGGGCATGGCAACTCGAGATACACTCTGTGGAGACTGCTGGCCTGGGTGGTTTGGGCCTTGGGGGGTTCCCCGCGTTCCATGTCAACCATGTTCCTGGGCACCTCTGGGTACTCATGGCTGTGATGAGTGGGGGCGGCGGGCCCGACGTGGCGTGGAGGTGGCAGCAGGGGCCAGCAGCGGTGGTGAGACACGGCAGCCTGGGAACGGCACCCGGGCAGGTGGCCCAGAGGAGACAGCCGCCCAGTACGCGGTCATCGCCATCGTCCCTGTCTTCTGCCTCATGGGGCTGTTGGGCATCCTGGTGTGCAACCTCCTCAAGCGGAAGGGCTACCACTGCACGGCGCACAAGGAGGTCGGGCCCGGCCCTGGAGGTGGAGGCAGTGGAATCAACCCTGCCTACCGGACTGAGGATGCCAATGAGGACACCATTGGGGTCCTGGTGCGCTTGATCACAGAGAAGAAAGAGAATGCTGCGGCCCTGGAGGAGCTGCTGAAAGAGTACCACAGCAAACAGCTGGTGCAGACGAGCCACAGGCCTGTGTCCAAGCTGCCGCCAGCGCCCCCGAACGTGCCACACATCTGCCCGCACCGCCACCATCTCCACACCGTGCAGGGCCTGGCCTCGCTCTCTGGCCCCTGCTGCTCCCGCTGTAGCCAGAAGAAGTGGCCCGAGGTGCTGCTGTCCCCTGAGGCTGTAGCCGCCACTACTCCTGTTCCCAGCCTTCTGCCTAACCCGACCAGGGTTCCCAAGGCCGGGGCCAAGGCAGGGCGTCAGGGCGAGATCACCATCTTGTCTGTGGGCAGGTTCCGCGTGGCTCGAATTCCTGAGCAGCGGACAAGTTCAATGGTGTCTGAGGTGAAGACCATCACGGAGGCTGGGCCCTCGTGGGGTGATCTCCCTGACTCCCCACAGCCTGGCCTCCCCCCTGAGCAGCAGGCCCTGCTAGGAAGTGGCGGAAGCCGTACAAAGTGGCTGAAGCCCCCAGCAGAGAACAAGGCCGAGGAGAACCGCTATGTGGTCCGGCTAAGTGAGAGCAACCTGGTCATCTGA
Amino sequence
MKPSLLCRPLSCFLMLLPWPLATLTSTTLWQCPPGEEPDLDPGQGTLCRPCPPGTFSAAWGSSPCQPHARCSLWRRLEAQVGMATRDTLCGDCWPGWFGPWGVPRVPCQPCSWAPLGTHGCDEWGRRARRGVEVAAGASSGGETRQPGNGTRAGGPEETAAQYAVIAIVPVFCLMGLLGILVCNLLKRKGYHCTAHKEVGPGPGGGGSGINPAYRTEDANEDTIGVLVRLITEKKENAAALEELLKEYHSKQLVQTSHRPVSKLPPAPPNVPHICPHRHHLHTVQGLASLSGPCCSRCSQKKWPEVLLSPEAVAATTPVPSLLPNPTRVPKAGAKAGRQGEITILSVGRFRVARIPEQRTSSMVSEVKTITEAGPSWGDLPDSPQPGLPPEQQALLGSGGSRTKWLKPPAENKAEENRYVVRLSESNLVI*