Linked Data
ClinVar Variation Id:
251279
ClinVar RCV Id:
RCV000238387
dbSNP Id:
rs879254561
PubMed:
PMID:11196104
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11105431_11105442del , CM000681.2:g.11105431_11105442del | GRCh38 |
| NC_000019.9:g.11216107_11216118del , CM000681.1:g.11216107_11216118del | GRCh37 |
| NC_000019.8:g.11077107_11077118del | NCBI36 |
| NG_009060.1:g.21051_21062del , LRG_274:g.21051_21062del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.783_794del | ENSP00000252444.6:p.Asp261_Asp264del | |
| ENST00000559340.2:c.525_536del | ENSP00000453696.2:p.Asp175_Asp178del | |
| ENST00000560467.2:c.525_536del | ENSP00000453513.2:p.Asp175_Asp178del | |
| ENST00000558518.6:c.525_536del MANE Select | ENSP00000454071.1:p.Asp175_Asp178del | |
| ENST00000252444.9:c.779_790del | ||
| ENST00000455727.6:c.314-1961_314-1950del | ENSP00000397829.2:n.314-1961_314-1950del | |
| ENST00000535915.5:c.402_413del | ENSP00000440520.1:p.Asp134_Asp137del | |
| ENST00000545707.5:c.314-1134_314-1123del | ENSP00000437639.1:n.314-1134_314-1123del | |
| ENST00000557933.5:c.525_536del | ENSP00000453557.1:p.Asp175_Asp178del | |
| ENST00000558013.5:c.525_536del | ENSP00000453346.1:p.Asp175_Asp178del | |
| ENST00000558518.5:c.525_536del | ENSP00000454071.1:p.Asp175_Asp178del | |
| ENST00000560467.1:c.125_136del | ||
| NM_000527.4:c.525_536del , LRG_274t1:c.525_536del | NP_000518.1:p.Asp175_Asp178del | |
| NM_001195798.1:c.525_536del | NP_001182727.1:p.Asp175_Asp178del | |
| NM_001195799.1:c.402_413del | NP_001182728.1:p.Asp134_Asp137del | |
| NM_001195800.1:c.314-1961_314-1950del | NP_001182729.1:n.314-1961_314-1950del | |
| NM_001195803.1:c.314-1134_314-1123del | NP_001182732.1:n.314-1134_314-1123del | |
| XM_011528010.1:c.525_536del | XP_011526312.1:p.Asp175_Asp178del | |
| XM_011528011.1:c.314-1134_314-1123del | XP_011526313.1:n.314-1134_314-1123del | |
| XR_244074.2:n.675_686del | ||
| XM_011528010.2:c.525_536del | XP_011526312.1:p.Asp175_Asp178del | |
| XR_001753685.2:n.642_653del | ||
| XR_001753686.2:n.642_653del | ||
| NM_000527.5:c.525_536del MANE Select | NP_000518.1:p.Asp175_Asp178del | |
| NM_001195798.2:c.525_536del | NP_001182727.1:p.Asp175_Asp178del | |
| NM_001195799.2:c.402_413del | NP_001182728.1:p.Asp134_Asp137del | |
| NM_001195800.2:c.314-1961_314-1950del | NP_001182729.1:n.314-1961_314-1950del | |
| NM_001195803.2:c.314-1134_314-1123del | NP_001182732.1:n.314-1134_314-1123del |