ENST00000620151.4 CT47C1
Information
- Transcript ID
- ENST00000620151.4
- Genome
- hg38
- Position
- chrX:119,072,993-119,076,765
- Strand
- +
- CDS length
- 975
- Amino acid length
- 325
- Gene symbol
- CT47C1
- Gene type
- protein-coding
- Gene description
- cancer/testis antigen family 47 member C1
- Gene Entrez Gene ID
- 727838
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 | 119,072,993 | 119,074,078 |
| 2 | 119,074,960 | 119,075,112 |
| 3 | 119,076,233 | 119,076,765 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 119,073,226 | 119,074,078 |
| 2 | CDS | 119,074,960 | 119,075,081 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chrX | 118,206,956 | 118,210,728 | Link |
CDS sequence
ATGTCTGCCACAGGGGATCAAGACCTGATCCAAGAGGACCAGGAGGCTCCAGTGAACCAGGAGGGAGCGCAGGCCGAGGCCGTAGGTGACCGGGAGGGCGGTGACTCTGGCCCCGACAGTGGCAACACTGTGGCCGGAGTCGCAGGGCCCATGAGAGGCCTCGGGGAGGAGGAGGGTGAGCAGGCGGCAGGCTTGGCCGCAGCCCCCGGGGGTGGGAACGCCGAGGAAGACTCAGAGATCAGGATAGTAGTGGAGATGGTGGAGGAGGAGGAGGATGAGGAGGAGGAAGAGGAGGAGGAGGAGGAAGAGAGGAACGAGGCGGACAACTTCGACTTGGTCGCGGCCGCCCGTCGCTACCCCATAAGAGGCTTTCGCATGGAGTTTCTGGACATGGTCCACTCCCTTCTCCTCCGCATCTATCACAACGACCACATCCTGATCAGGATGCGTGGCGGCCGCCTGATGCGGAGGCGCCGCACTGCGGCGCCCAGTGGCTCAGAAGAGCCCCGGCTGTTGCTGGTGCATGAGAGGCTGGGCGTGGGGGCCGCGGGTCCTGAGGGCGAGGGCCTGGGCCTGCTCCAGGAGGCCGCGTTGGTCCCAGAGCCTGAGGTGCCAGCAGACCTGGCCGAGATGGCCAGGGAGCCTGCAGAAGAGCCCGCAGAGGAGGCCTCAGAGAAGCCCACAGAGGAGGCCGCAGAAGAGCCCGCAGAGGAGGCCTCAGAGAAGCCCACAGAGGAGGCCGCAGAGGAGGAGCTCGCAGAGGAGGCCGCAGAGGAACCGGCCAAAGAGGAACCGGCTGCAGAGGAGGAGTCCGCAGAGGAACCGGCCACAGAGGAGGCTGCTGCCCCTGAGGAAGTCACTAAATATCAGCATGAAAAGTGGGATGAAGAGGCCCAAGATGCTGCAGGCAAGGAAGAGAAAGAAGAGAAAGAGAAGGATGCTGAAAACAAGGTGAAGAACTCCAAAGGGACCTAG
Amino sequence
MSATGDQDLIQEDQEAPVNQEGAQAEAVGDREGGDSGPDSGNTVAGVAGPMRGLGEEEGEQAAGLAAAPGGGNAEEDSEIRIVVEMVEEEEDEEEEEEEEEEERNEADNFDLVAAARRYPIRGFRMEFLDMVHSLLLRIYHNDHILIRMRGGRLMRRRRTAAPSGSEEPRLLLVHERLGVGAAGPEGEGLGLLQEAALVPEPEVPADLAEMAREPAEEPAEEASEKPTEEAAEEPAEEASEKPTEEAAEEELAEEAAEEPAKEEPAAEEESAEEPATEEAAAPEEVTKYQHEKWDEEAQDAAGKEEKEEKEKDAENKVKNSKGT*