Linked Data
ClinVar Variation Id:
2848137
ClinVar RCV Id:
RCV003652576
MyVariant Identifiers:
chr17:g.42979823C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44902455C>T , CM000679.2:g.44902455C>T | GRCh38 |
| NC_000017.10:g.42979823C>T , CM000679.1:g.42979823C>T | GRCh37 |
| NC_000017.9:g.40335349C>T | NCBI36 |
| NG_032674.1:g.2171G>A | |
| NG_032792.1:g.7744C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000417826.3:c.367C>T (CCDC103) MANE Select | ENSP00000391692.2:p.Leu123= | |
| ENST00000331733.4:c.-1375C>T (FAM187A) | ENSP00000329499.4:n.-1375C>T | |
| ENST00000357776.6:c.367C>T (CCDC103) | ENSP00000350420.2:p.Leu123= | |
| ENST00000410006.6:c.367C>T (CCDC103) | ENSP00000387252.1:p.Leu123= | |
| ENST00000410027.5:c.*117C>T (CCDC103) | ENSP00000386640.1:n.*117C>T | |
| ENST00000412523.3:c.367C>T (FAM187A) | ENSP00000391869.3:p.Leu123= | |
| ENST00000417826.2:c.367C>T (CCDC103) | ENSP00000391692.2:p.Leu123= | |
| NM_001258395.1:c.367C>T (CCDC103) | NP_001245324.1:p.Leu123= | |
| NM_001258396.1:c.367C>T (CCDC103) | NP_001245325.1:p.Leu123= | |
| NM_001258397.1:c.*117C>T (CCDC103) | NP_001245326.1:n.*117C>T | |
| NM_001258398.1:c.*56C>T (CCDC103) | NP_001245327.1:n.*56C>T | |
| NM_001258399.1:c.*56C>T (CCDC103) | NP_001245328.1:n.*56C>T | |
| NM_213607.2:c.367C>T (CCDC103) | NP_998772.1:p.Leu123= | |
| NM_001258395.2:c.367C>T (CCDC103) | NP_001245324.1:p.Leu123= | |
| NM_001258396.2:c.367C>T (CCDC103) | NP_001245325.1:p.Leu123= | |
| NM_001258398.2:c.*56C>T (CCDC103) | NP_001245327.1:n.*56C>T | |
| NM_001258399.2:c.*56C>T (CCDC103) | NP_001245328.1:n.*56C>T | |
| NM_213607.3:c.367C>T (CCDC103) MANE Select | NP_998772.1:p.Leu123= | |
| NM_001258397.3:c.*117C>T (CCDC103) | NP_001245326.1:n.*117C>T | |
| NM_001258398.3:c.*56C>T (CCDC103) | NP_001245327.1:n.*56C>T |