ENST00000372653.5 NFYC
Information
- Transcript ID
- ENST00000372653.5
- Genome
- hg38
- Position
- chr1:40,692,013-40,771,106
- Strand
- +
- CDS length
- 906
- Amino acid length
- 302
- Gene symbol
- NFYC
- Gene type
- protein-coding
- Gene description
- nuclear transcription factor Y subunit gamma
- Gene Entrez Gene ID
- 4802
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| 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 | 40,692,013 | 40,692,200 |
| 2 | 40,695,606 | 40,695,745 |
| 3 | 40,712,398 | 40,712,469 |
| 4 | 40,721,606 | 40,721,704 |
| 5 | 40,723,208 | 40,723,274 |
| 6 | 40,723,689 | 40,723,792 |
| 7 | 40,738,836 | 40,738,948 |
| 8 | 40,747,534 | 40,747,605 |
| 9 | 40,749,573 | 40,749,686 |
| 10 | 40,753,151 | 40,753,246 |
| 11 | 40,758,121 | 40,758,294 |
| 12 | 40,762,990 | 40,763,046 |
| 13 | 40,766,596 | 40,766,703 |
| 14 | 40,769,356 | 40,769,415 |
| 15 | 40,770,709 | 40,771,106 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 7 | CDS | 40,738,844 | 40,738,948 |
| 8 | CDS | 40,747,534 | 40,747,605 |
| 9 | CDS | 40,749,573 | 40,749,686 |
| 10 | CDS | 40,753,151 | 40,753,246 |
| 11 | CDS | 40,758,121 | 40,758,294 |
| 12 | CDS | 40,762,990 | 40,763,046 |
| 13 | CDS | 40,766,596 | 40,766,703 |
| 14 | CDS | 40,769,356 | 40,769,415 |
| 15 | CDS | 40,770,709 | 40,770,828 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr1 | 41,157,685 | 41,236,778 | Link |
CDS sequence
ATGTCCACAGAAGGAGGATTTGGTGGTACTAGCAGCAGTGATGCCCAGCAAAGCCTACAGTCGTTCTGGCCTCGGGTCATGGAAGAAATCCGGAATTTAACAGTGAAAGACTTCCGAGTGCAGGAACTCCCACTGGCTCGTATTAAGAAGATTATGAAACTGGATGAAGATGTGAAGATGATCAGTGCAGAAGCGCCTGTACTCTTTGCCAAGGCAGCCCAGATTTTTATCACAGAGTTGACTCTTCGAGCCTGGATTCACACAGAAGATAACAAGCGCCGGACTCTACAGAGAAATGATATCGCCATGGCAATTACAAAATTTGATCAGTTTGATTTTCTCATCGATATTGTTCCAAGAGATGAACTGAAACCTCCAAAGCGTCAGGAGGAGGTGCGCCAGTCTGTAACTCCTGCCGAGCCAGTCCAGTACTATTTCACGCTGGCTCAGCAACCCACCGCTGTCCAAGTCCAGGGCCAGCAGCAAGGCCAGCAGACCACCAGCTCCACGACCACCATCCAGCCTGGGCAGATCATCATCGCACAGCCTCAGCAGGGCCAGACCATGCAGGTGATGCAGCAGATCATCACTAACACAGGAGAGATCCAGCAGATCCCGGTGCAGCTGAATGCCGGCCAGCTGCAGTATATCCGCTTAGCCCAGCCTGTATCAGGCACTCAAGTTGTGCAGGGACAGATCCAGACACTTGCCACCAATGCTCAACAGATTACACAGACAGAGGTCCAGCAAGGACAGCAGCAGTTCAGCCAGTTCACAGATGGACAGCAGCTCTACCAGATCCAGCAAGTCACCATGCCTGCGGGCCAGGACCTCGCCCAGCCCATGTTCATCCAGTCAGCCAACCAGCCCTCCGACGGGCAGGCCCCCCAGGTGACCGGCGACTGA
Amino sequence
MSTEGGFGGTSSSDAQQSLQSFWPRVMEEIRNLTVKDFRVQELPLARIKKIMKLDEDVKMISAEAPVLFAKAAQIFITELTLRAWIHTEDNKRRTLQRNDIAMAITKFDQFDFLIDIVPRDELKPPKRQEEVRQSVTPAEPVQYYFTLAQQPTAVQVQGQQQGQQTTSSTTTIQPGQIIIAQPQQGQTMQVMQQIITNTGEIQQIPVQLNAGQLQYIRLAQPVSGTQVVQGQIQTLATNAQQITQTEVQQGQQQFSQFTDGQQLYQIQQVTMPAGQDLAQPMFIQSANQPSDGQAPQVTGD*