ENST00000454109.1 C2CD4D
Information
- Transcript ID
- ENST00000454109.1
- Genome
- hg38
- Position
- chr1:151,837,819-151,840,557
- Strand
- -
- CDS length
- 1,062
- Amino acid length
- 354
- Gene symbol
- C2CD4D
- Gene type
- protein-coding
- Gene description
- C2 calcium dependent domain containing 4D
- Gene Entrez Gene ID
- 100191040
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| 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 |
|---|---|---|
| 2 | 151,837,819 | 151,839,220 |
| 1 | 151,840,203 | 151,840,557 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 2 | CDS | 151,837,928 | 151,838,989 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr1 | 151,810,295 | 151,813,033 | Link |
CDS sequence
ATGTGGCTCTTGGAAAAAGCTGGCTATAAGGTGGGGGCCGCGGAGCCTGCGGCCCGTTGGGCGCCTTCCGGCCTGTTCTCCAAGCGTCGCGCCCCGGGCCCGCCCACAAGCGCCTGCCCCAACGTCCTCACCCCGGATCGCATCCCGCAGTTCTTCATCCCGCCTCGGCTCCCGGACCCGGGCGGCGCAGTGCCCGCGGCCCGGCGGCACGTGGCGGGGCGCGGCCTCCCCGCGACCTGCTCGCTGCCTCACCTGGCGGGCCGCGAAGGCTGGGCCTTCCTGCCCGAGAGCCCGCACACGCGCCGGCGGGAATCCCTGTTCCACGGGCCGCCACCTGCCCCGGCCGGGGGACTCCCCGCGGCGCAGTCCCGGCTGCACGTCTCCGCCCCGGACCTGCGCCTCTGCCGGGCCCCCGACAGCGACACGGCCTCGTCGCCGGACTCGTCGCCCTTCGGCTCCCCGCGGCCAGGCCTGGGCCGGCGCCGGGTGTCCAGGCCTCACTCTCTGTCCCCAGAAAAAGCGAGCTCGGCCGATACCAGCCCGCACTCGCCGCGCCGCGCCGGGCCGCCCACGCCGCCGCTCTTCCACCTGGACTTCCTGTGCTGCCAGCTGCGGCCCACGCGCGAGAGCGTGCTGCGCCTGGGGCCCCGCGGCGGGCAGCTGCGGCTCTCCACCGAATATCAGGCCGGGCCCGGGCGGCTGCGGCTGCGCCTAGTGAGCGCCGAGGGCCTGCCCCGGCCGCGGTCCCGCCCCGGGAGCGGCGGCGGCGGCTGCTGTGTGGTGCTGAGGCTGCGGCCCCGCGTCCGGCCGCGGGAGCAGCAGAGCCGCGTGGTCAAGTGCAGCGCCAACCCCATCTTCAACGAGGATTTCTTTTTCGACGGGCTCGGCCCCCCGGACCTGGCCGCCCGCAGCCTGAGAGCCAAGGTGCTAGACAGGGGCGCGGGACTTCGCAGGGATGTGCTGCTGGGGGAGTGCGAGACGCCCCTCATTGCGCTGCTGCCCCCGCTGGGTGGGGGACTAGGTCCCGGGTCATCCCTGGCGCCCACCCATCTCAGCCTGTAG
Amino sequence
MWLLEKAGYKVGAAEPAARWAPSGLFSKRRAPGPPTSACPNVLTPDRIPQFFIPPRLPDPGGAVPAARRHVAGRGLPATCSLPHLAGREGWAFLPESPHTRRRESLFHGPPPAPAGGLPAAQSRLHVSAPDLRLCRAPDSDTASSPDSSPFGSPRPGLGRRRVSRPHSLSPEKASSADTSPHSPRRAGPPTPPLFHLDFLCCQLRPTRESVLRLGPRGGQLRLSTEYQAGPGRLRLRLVSAEGLPRPRSRPGSGGGGCCVVLRLRPRVRPREQQSRVVKCSANPIFNEDFFFDGLGPPDLAARSLRAKVLDRGAGLRRDVLLGECETPLIALLPPLGGGLGPGSSLAPTHLSL*