Linked Data
ClinVar Variation Id:
251343
ClinVar RCV Id:
RCV000238486
dbSNP Id:
rs879254608
PubMed:
PMID:11810272
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11105551_11105552del , CM000681.2:g.11105551_11105552del | GRCh38 |
| NC_000019.9:g.11216227_11216228del , CM000681.1:g.11216227_11216228del | GRCh37 |
| NC_000019.8:g.11077227_11077228del | NCBI36 |
| NG_009060.1:g.21171_21172del , LRG_274:g.21171_21172del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.903_904del | ENSP00000252444.6:p.Cys302Ter | |
| ENST00000559340.2:c.645_646del | ENSP00000453696.2:p.Cys216Ter | |
| ENST00000560467.2:c.645_646del | ENSP00000453513.2:p.Cys216Ter | |
| ENST00000558518.6:c.645_646del MANE Select | ENSP00000454071.1:p.Cys216Ter | |
| ENST00000252444.9:c.899_900del | ||
| ENST00000455727.6:c.314-1841_314-1840del | ENSP00000397829.2:n.314-1841_314-1840del | |
| ENST00000535915.5:c.522_523del | ENSP00000440520.1:p.Cys175Ter | |
| ENST00000545707.5:c.314-1014_314-1013del | ENSP00000437639.1:n.314-1014_314-1013del | |
| ENST00000557933.5:c.645_646del | ENSP00000453557.1:p.Cys216Ter | |
| ENST00000558013.5:c.645_646del | ENSP00000453346.1:p.Cys216Ter | |
| ENST00000558518.5:c.645_646del | ENSP00000454071.1:p.Cys216Ter | |
| ENST00000560467.1:c.245_246del | ||
| NM_000527.4:c.645_646del , LRG_274t1:c.645_646del | NP_000518.1:p.Cys216Ter | |
| NM_001195798.1:c.645_646del | NP_001182727.1:p.Cys216Ter | |
| NM_001195799.1:c.522_523del | NP_001182728.1:p.Cys175Ter | |
| NM_001195800.1:c.314-1841_314-1840del | NP_001182729.1:n.314-1841_314-1840del | |
| NM_001195803.1:c.314-1014_314-1013del | NP_001182732.1:n.314-1014_314-1013del | |
| XM_011528010.1:c.645_646del | XP_011526312.1:p.Cys216Ter | |
| XM_011528011.1:c.314-1014_314-1013del | XP_011526313.1:n.314-1014_314-1013del | |
| XR_244074.2:n.795_796del | ||
| XM_011528010.2:c.645_646del | XP_011526312.1:p.Cys216Ter | |
| XR_001753685.2:n.762_763del | ||
| XR_001753686.2:n.762_763del | ||
| NM_000527.5:c.645_646del MANE Select | NP_000518.1:p.Cys216Ter | |
| NM_001195798.2:c.645_646del | NP_001182727.1:p.Cys216Ter | |
| NM_001195799.2:c.522_523del | NP_001182728.1:p.Cys175Ter | |
| NM_001195800.2:c.314-1841_314-1840del | NP_001182729.1:n.314-1841_314-1840del | |
| NM_001195803.2:c.314-1014_314-1013del | NP_001182732.1:n.314-1014_314-1013del |