ENST00000422000.5 CCDC77
Information
- Transcript ID
- ENST00000422000.5
- Genome
- hg38
- Position
- chr12:389,350-442,638
- Strand
- +
- CDS length
- 1,371
- Amino acid length
- 457
- Gene symbol
- CCDC77
- Gene type
- protein-coding
- Gene description
- coiled-coil domain containing 77
- Gene Entrez Gene ID
- 84318
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 | 389,350 | 389,486 |
2 | 405,511 | 405,564 |
3 | 411,747 | 411,978 |
4 | 418,494 | 418,636 |
5 | 428,769 | 428,865 |
6 | 430,664 | 430,736 |
7 | 431,866 | 431,954 |
8 | 433,174 | 433,322 |
9 | 438,335 | 438,554 |
10 | 440,617 | 440,742 |
11 | 440,844 | 440,996 |
12 | 441,774 | 442,638 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
3 | CDS | 411,805 | 411,978 |
4 | CDS | 418,494 | 418,636 |
5 | CDS | 428,769 | 428,865 |
6 | CDS | 430,664 | 430,736 |
7 | CDS | 431,866 | 431,954 |
8 | CDS | 433,174 | 433,322 |
9 | CDS | 438,335 | 438,554 |
10 | CDS | 440,617 | 440,742 |
11 | CDS | 440,844 | 440,996 |
12 | CDS | 441,774 | 441,920 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr12 | 498,516 | 551,804 | Link |
CDS sequence
ATGGCAGATTCACTGGAGTCAACCCCCTTGCCTTCCCCCGAAGATCGTCTGGCCAAACTCCATCCTTCTAAGGAGCTCCTGGAATATTATCAAAAGAAGATGGCTGAGTGTGAGGCAGAAAATGAGGACTTGCTGAAGAAACTGGAACTCTACAAAGAAGCTTGTGAAGGACAGCATAAACTTGAATGTGATTTGCAGCAGAGGGAGGAAGAGATTGCTGAATTGCAGAAAGCTCTAAGTGATATGCAGGTCTGCCTCTTCCAGGAACGGGAACATGTTTTACGCCTCTACTCAGAAAATGACCGACTGAGAATCAGGGAGCTAGAAGACAAGAAAAAGATTCAGAATCTCTTGGCTCTTGTGGGAACAGATGCTGGAGAAGTGACCTATTTTTGTAAGGAGCCTCCTCACAAAGTCACCATTCTCCAAAAGACTATCCAGGCTGTAGGTGAATGTGAGCAGAGTGAATCTTCAGCTTTCAAAGCAGATCCTAAAATAAGCAAAAGAAGACCATCGAGAGAGAGAAAAGAAAGTTCTGAGCATTACCAAAGAGACATACAGACACTCATCCTACAGGTGGAAGCACTGCAGGCTCAGCTGGGAGAGCAGACCAAACTTTCTCGAGAACAAATTGAAGGGCTCATCGAGGACAGACGGATTCACCTTGAGGAAATACAAGTTCAGCACCAGAGAAATCAGAACAAAATCAAAGAGCTAACCAAAAATCTTCACCACACCCAAGAACTGCTCTATGAGAGCACCAAAGATTTTCTGCAACTCAGATCTGAAAACCAAAATAAAGAGAAGTCATGGATGCTTGAAAAAGATAATTTGATGTCAAAGATTAAGCAATATAGGGTGCAGTGTAAGAAGAAAGAAGATAAAATTGGAAAAGTGTTGCCCGTTATGCATGAGAGTCACCATGCTCAAAGTGAATATATTAAGTCCCTAAAAGATAAGTTAGTACAAGAGAAAAAGCTGTCCAATATGTACCAAGAGCAGTGCATTTCCTTAGAAGAAGAACTTGCCCGAATTCGTGAGGAAGAGGGAATGAGGAGAGAGATCTTCAAGGATCGCACTAACAAGATGGGGAAGCGTTTACAGATAATGACAAAACGCTATGAGGCATTGGAGCGTCGACGTATCCTGGAAGTAGAAGGCTTTAAGACAGATATTAAAGTTCTCCGACAGAAACTGAAAGACTTGGAGCAAATGTTGTATAAGGCAACAGTTAATGCCCGGGCAAACCAGGATCTTGCCCTTCTGTGTGAGGTCCGTGACAGCAATAGACGGGCACATAAGATACAAGGAGAACTGAAGAATCTTAAGTCGAAAGTGTTTGGTCTGGAGAATGAACTTAGACTCTGTTAA
Amino sequence
MADSLESTPLPSPEDRLAKLHPSKELLEYYQKKMAECEAENEDLLKKLELYKEACEGQHKLECDLQQREEEIAELQKALSDMQVCLFQEREHVLRLYSENDRLRIRELEDKKKIQNLLALVGTDAGEVTYFCKEPPHKVTILQKTIQAVGECEQSESSAFKADPKISKRRPSRERKESSEHYQRDIQTLILQVEALQAQLGEQTKLSREQIEGLIEDRRIHLEEIQVQHQRNQNKIKELTKNLHHTQELLYESTKDFLQLRSENQNKEKSWMLEKDNLMSKIKQYRVQCKKKEDKIGKVLPVMHESHHAQSEYIKSLKDKLVQEKKLSNMYQEQCISLEEELARIREEEGMRREIFKDRTNKMGKRLQIMTKRYEALERRRILEVEGFKTDIKVLRQKLKDLEQMLYKATVNARANQDLALLCEVRDSNRRAHKIQGELKNLKSKVFGLENELRLC*