Linked Data
ClinVar Variation Id:
375242
ClinVar RCV Id:
RCV000416289
dbSNP Id:
rs1057519330
PubMed:
PMID:27884168
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108249059del , CM000673.2:g.108249059del | GRCh38 |
| NC_000011.9:g.108119786del , CM000673.1:g.108119786del | GRCh37 |
| NC_000011.8:g.107624996del | NCBI36 |
| NG_009830.1:g.31228del , LRG_135:g.31228del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000452508.7:c.1192del | ENSP00000388058.2:p.Asp398IlefsTer22 | |
| ENST00000713593.1:c.*663del | ENSP00000518889.1:n.*663del | |
| ENST00000278616.9:c.1192del | ENSP00000278616.4:p.Asp398IlefsTer22 | |
| ENST00000682516.1:n.1326del | ||
| ENST00000682956.1:n.1326del | ||
| ENST00000683174.1:n.1342del | ||
| ENST00000683605.1:n.687del | ||
| ENST00000684037.1:c.*127del | ENSP00000508245.1:n.*127del | |
| ENST00000684061.1:n.1326del | ||
| ENST00000684179.1:n.1161del | ||
| ENST00000527805.6:c.1192del | ENSP00000435747.2:p.Asp398IlefsTer22 | |
| ENST00000675595.1:c.1027del | ENSP00000502563.1:p.Asp343IlefsTer22 | |
| ENST00000675843.1:c.1192del MANE Select | ENSP00000501606.1:p.Asp398IlefsTer22 | |
| ENST00000278616.8:c.1192del | ENSP00000278616.4:p.Asp398IlefsTer22 | |
| ENST00000452508.6:c.1192del | ENSP00000388058.2:p.Asp398IlefsTer22 | |
| ENST00000527805.5:c.1192del | ENSP00000435747.1:p.Asp398IlefsTer22 | |
| NM_000051.3:c.1192del , LRG_135t1:c.1192del | NP_000042.3:p.Asp398IlefsTer22 | |
| XM_005271561.3:c.1192del | XP_005271618.2:p.Asp398IlefsTer22 | |
| XM_005271562.3:c.1192del | XP_005271619.2:p.Asp398IlefsTer22 | |
| XM_006718843.2:c.1192del | XP_006718906.1:p.Asp398IlefsTer22 | |
| XM_011542840.1:c.1192del | XP_011541142.1:p.Asp398IlefsTer22 | |
| XM_011542841.1:c.1192del | XP_011541143.1:p.Asp398IlefsTer22 | |
| XM_011542842.1:c.1027del | XP_011541144.1:p.Asp343IlefsTer22 | |
| XM_011542843.1:c.1192del | XP_011541145.1:p.Asp398IlefsTer22 | |
| XM_011542844.1:c.148del | XP_011541146.1:p.Asp50IlefsTer22 | |
| XM_011542845.1:c.-73-1642del | XP_011541147.1:n.-73-1642del | |
| XM_011542846.1:c.1192del | XP_011541148.1:p.Asp398IlefsTer22 | |
| NM_001351834.1:c.1192del | NP_001338763.1:p.Asp398IlefsTer22 | |
| XM_005271562.5:c.1192del | XP_005271619.2:p.Asp398IlefsTer22 | |
| XM_006718843.4:c.1192del | XP_006718906.1:p.Asp398IlefsTer22 | |
| XM_011542840.3:c.1192del | XP_011541142.1:p.Asp398IlefsTer22 | |
| XM_011542842.3:c.1027del | XP_011541144.1:p.Asp343IlefsTer22 | |
| XM_011542843.2:c.1192del | XP_011541145.1:p.Asp398IlefsTer22 | |
| XM_011542844.3:c.148del | XP_011541146.1:p.Asp50IlefsTer22 | |
| XM_011542845.2:c.-73-1642del | XP_011541147.1:n.-73-1642del | |
| XM_017017789.2:c.1192del | XP_016873278.1:p.Asp398IlefsTer22 | |
| XM_017017790.2:c.1192del | XP_016873279.1:p.Asp398IlefsTer22 | |
| XM_017017791.1:c.1192del | XP_016873280.1:p.Asp398IlefsTer22 | |
| XM_017017792.2:c.1192del | XP_016873281.1:p.Asp398IlefsTer22 | |
| XR_002957150.1:n.1925del | ||
| NM_001351834.2:c.1192del | NP_001338763.1:p.Asp398IlefsTer22 | |
| NM_000051.4:c.1192del MANE Select | NP_000042.3:p.Asp398IlefsTer22 |