ENST00000541430.6 CELF5
Information
- Transcript ID
- ENST00000541430.6
- Genome
- hg19
- Position
- chr19:3,224,702-3,296,334
- Strand
- +
- CDS length
- 1,230
- Amino acid length
- 410
- Gene symbol
- CELF5
- Gene type
- protein-coding
- Gene description
- CUGBP Elav-like family member 5
- Gene Entrez Gene ID
- 60680
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 | 3,224,702 | 3,224,996 |
2 | 3,250,983 | 3,251,065 |
3 | 3,273,870 | 3,273,921 |
4 | 3,275,854 | 3,275,982 |
5 | 3,278,029 | 3,278,108 |
6 | 3,281,197 | 3,281,343 |
7 | 3,282,124 | 3,282,265 |
8 | 3,282,425 | 3,282,496 |
9 | 3,284,900 | 3,284,962 |
10 | 3,285,940 | 3,286,023 |
11 | 3,290,270 | 3,290,372 |
12 | 3,293,317 | 3,296,334 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 3,224,738 | 3,224,996 |
2 | CDS | 3,250,983 | 3,251,065 |
3 | CDS | 3,273,870 | 3,273,921 |
4 | CDS | 3,275,854 | 3,275,982 |
5 | CDS | 3,278,029 | 3,278,108 |
6 | CDS | 3,281,197 | 3,281,343 |
7 | CDS | 3,282,124 | 3,282,265 |
8 | CDS | 3,282,425 | 3,282,496 |
9 | CDS | 3,284,900 | 3,284,962 |
10 | CDS | 3,285,940 | 3,286,023 |
11 | CDS | 3,290,270 | 3,290,372 |
12 | CDS | 3,293,317 | 3,293,332 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr19 | 3,224,704 | 3,296,336 | Link |
CDS sequence
ATGGCCCGCCTGACGGAGAGCGAGGCGCGCCGGCAGCAGCAGCAGCTCCTGCAGCCGCGGCCCTCGCCCGTGGGCAGCAGCGGGCCCGAGCCCCCCGGGGGGCAGCCCGACGGCATGAAGGACCTGGACGCCATCAAACTCTTCGTGGGCCAGATCCCGCGGCACCTGGACGAGAAGGACCTCAAGCCGCTCTTCGAGCAGTTCGGCCGCATCTACGAGCTCACGGTGCTCAAAGACCCCTACACGGGGATGCACAAAGGCTGTGCCTTCCTCACCTACTGTGCCAGGGATTCCGCCATCAAAGCTCAGACTGCCCTGCACGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGA
Amino sequence
MARLTESEARRQQQQLLQPRPSPVGSSGPEPPGGQPDGMKDLDAIKLFVGQIPRHLDEKDLKPLFEQFGRIYELTVLKDPYTGMHKGCAFLTYCARDSAIKAQTALHEQKTLPGMARPIQVKPADSESRGGRDRKLFVGMLNKQQSEEDVLRLFQPFGVIDECTVLRGPDGSSKGCAFVKFSSHTEAQAAIHALHGSQTMPGASSSLVVKFADTDKERTLRRMQQMVGQLGILTPSLTLPFSPYSAYAQALMQQQTTVLSTSGSYLSPGVAFSPCHIQQIGAVSLNGLPATPIAPASGVVPFPGGHPALETVYANGLVPYPAQSPTVAETLHPAFSGVQQYTAMYPTAAITPIAHSVPQPPPLLQQQQREGVWRHGADADVPTLRQYHFLQGVYGSSYQPEQVFRLREL*