Linked Data
ClinVar Variation Id:
1560623
ClinVar RCV Id:
RCV002209209
dbSNP Id:
rs2147286811
COSMIC:
COSM4480267
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11129526C>T , CM000681.2:g.11129526C>T | GRCh38 |
| NC_000019.9:g.11240202C>T , CM000681.1:g.11240202C>T | GRCh37 |
| NC_000019.8:g.11101202C>T | NCBI36 |
| NG_009060.1:g.45146C>T , LRG_274:g.45146C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2661C>T | ENSP00000252444.6:p.Phe887= | |
| ENST00000559340.2:c.*472C>T | ENSP00000453696.2:n.*472C>T | |
| ENST00000560467.2:c.2283C>T | ENSP00000453513.2:p.Phe761= | |
| ENST00000558518.6:c.2403C>T MANE Select | ENSP00000454071.1:p.Phe801= | |
| ENST00000252444.9:c.2657C>T | ||
| ENST00000455727.6:c.1899C>T | ENSP00000397829.2:p.Phe633= | |
| ENST00000535915.5:c.2280C>T | ENSP00000440520.1:p.Phe760= | |
| ENST00000545707.5:c.1869C>T | ENSP00000437639.1:p.Phe623= | |
| ENST00000557933.5:c.2465C>T | ENSP00000453557.1:p.Ser822Phe | |
| ENST00000558013.5:c.2403C>T | ENSP00000453346.1:p.Phe801= | |
| ENST00000558518.5:c.2403C>T | ENSP00000454071.1:p.Phe801= | |
| ENST00000560628.1:n.108+1872C>T | ||
| NM_000527.4:c.2403C>T , LRG_274t1:c.2403C>T | NP_000518.1:p.Phe801= | |
| NM_001195798.1:c.2403C>T | NP_001182727.1:p.Phe801= | |
| NM_001195799.1:c.2280C>T | NP_001182728.1:p.Phe760= | |
| NM_001195800.1:c.1899C>T | NP_001182729.1:p.Phe633= | |
| NM_001195803.1:c.1869C>T | NP_001182732.1:p.Phe623= | |
| XM_011528010.1:c.2325C>T | XP_011526312.1:p.Phe775= | |
| XM_011528011.1:c.2022C>T | XP_011526313.1:p.Phe674= | |
| XR_244074.2:n.2413C>T | ||
| XM_011528010.2:c.2325C>T | XP_011526312.1:p.Phe775= | |
| XR_001753685.2:n.2737C>T | ||
| XR_001753686.2:n.2380C>T | ||
| NM_000527.5:c.2403C>T MANE Select | NP_000518.1:p.Phe801= | |
| NM_001195798.2:c.2403C>T | NP_001182727.1:p.Phe801= | |
| NM_001195799.2:c.2280C>T | NP_001182728.1:p.Phe760= | |
| NM_001195800.2:c.1899C>T | NP_001182729.1:p.Phe633= | |
| NM_001195803.2:c.1869C>T | NP_001182732.1:p.Phe623= |