Linked Data
ClinVar Variation Id:
251263
ClinVar RCV Id:
RCV000238551
dbSNP Id:
rs879254551
PubMed:
PMID:15241806
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11105414_11105415insC , CM000681.2:g.11105414_11105415insC | GRCh38 |
| NC_000019.9:g.11216090_11216091insC , CM000681.1:g.11216090_11216091insC | GRCh37 |
| NC_000019.8:g.11077090_11077091insC | NCBI36 |
| NG_009060.1:g.21034_21035insC , LRG_274:g.21034_21035insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.766_767insC | ENSP00000252444.6:p.Asp256AlafsTer10 | |
| ENST00000559340.2:c.508_509insC | ENSP00000453696.2:p.Asp170AlafsTer10 | |
| ENST00000560467.2:c.508_509insC | ENSP00000453513.2:p.Asp170AlafsTer10 | |
| ENST00000558518.6:c.508_509insC MANE Select | ENSP00000454071.1:p.Asp170AlafsTer10 | |
| ENST00000252444.9:c.762_763insC | ||
| ENST00000455727.6:c.314-1978_314-1977insC | ENSP00000397829.2:n.314-1978_314-1977insC | |
| ENST00000535915.5:c.385_386insC | ENSP00000440520.1:p.Asp129AlafsTer10 | |
| ENST00000545707.5:c.314-1151_314-1150insC | ENSP00000437639.1:n.314-1151_314-1150insC | |
| ENST00000557933.5:c.508_509insC | ENSP00000453557.1:p.Asp170AlafsTer10 | |
| ENST00000558013.5:c.508_509insC | ENSP00000453346.1:p.Asp170AlafsTer10 | |
| ENST00000558518.5:c.508_509insC | ENSP00000454071.1:p.Asp170AlafsTer10 | |
| ENST00000560467.1:c.108_109insC | ||
| NM_000527.4:c.508_509insC , LRG_274t1:c.508_509insC | NP_000518.1:p.Asp170AlafsTer10 | |
| NM_001195798.1:c.508_509insC | NP_001182727.1:p.Asp170AlafsTer10 | |
| NM_001195799.1:c.385_386insC | NP_001182728.1:p.Asp129AlafsTer10 | |
| NM_001195800.1:c.314-1978_314-1977insC | NP_001182729.1:n.314-1978_314-1977insC | |
| NM_001195803.1:c.314-1151_314-1150insC | NP_001182732.1:n.314-1151_314-1150insC | |
| XM_011528010.1:c.508_509insC | XP_011526312.1:p.Asp170AlafsTer10 | |
| XM_011528011.1:c.314-1151_314-1150insC | XP_011526313.1:n.314-1151_314-1150insC | |
| XR_244074.2:n.658_659insC | ||
| XM_011528010.2:c.508_509insC | XP_011526312.1:p.Asp170AlafsTer10 | |
| XR_001753685.2:n.625_626insC | ||
| XR_001753686.2:n.625_626insC | ||
| NM_000527.5:c.508_509insC MANE Select | NP_000518.1:p.Asp170AlafsTer10 | |
| NM_001195798.2:c.508_509insC | NP_001182727.1:p.Asp170AlafsTer10 | |
| NM_001195799.2:c.385_386insC | NP_001182728.1:p.Asp129AlafsTer10 | |
| NM_001195800.2:c.314-1978_314-1977insC | NP_001182729.1:n.314-1978_314-1977insC | |
| NM_001195803.2:c.314-1151_314-1150insC | NP_001182732.1:n.314-1151_314-1150insC |