Linked Data
ClinVar Variation Id:
141742
dbSNP Id:
rs587781978
ExAC:
11:108115639 CT / C
gnomAD v2:
11-108115639-CT-C
gnomAD v4:
11-108244912-CT-C
MyVariant Identifiers:
chr11:g.108115642del (hg19)
chr11:g.108115640del (hg19)
chr11:g.108244915del (hg38)
chr11:g.108244913del (hg38)
ERepo:
CA166283/MONDO:0016419/020
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108244915del , CM000673.2:g.108244915del | GRCh38 |
| NC_000011.9:g.108115642del , CM000673.1:g.108115642del | GRCh37 |
| NC_000011.8:g.107620852del | NCBI36 |
| NG_009830.1:g.27084del , LRG_135:g.27084del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000452508.7:c.790del | ENSP00000388058.2:p.Tyr264IlefsTer12 | |
| ENST00000713593.1:c.*261del | ENSP00000518889.1:n.*261del | |
| ENST00000278616.9:c.790del | ENSP00000278616.4:p.Tyr264IlefsTer12 | |
| ENST00000682430.1:n.889del | ||
| ENST00000682516.1:n.924del | ||
| ENST00000682956.1:n.924del | ||
| ENST00000683100.1:n.3137del | ||
| ENST00000683174.1:n.940del | ||
| ENST00000683605.1:n.285del | ||
| ENST00000684037.1:c.790del | ENSP00000508245.1:p.Tyr264IlefsTer12 | |
| ENST00000684061.1:n.924del | ||
| ENST00000684179.1:n.759del | ||
| ENST00000527805.6:c.790del | ENSP00000435747.2:p.Tyr264IlefsTer12 | |
| ENST00000675595.1:c.625del | ENSP00000502563.1:p.Tyr209IlefsTer12 | |
| ENST00000675843.1:c.790del MANE Select | ENSP00000501606.1:p.Tyr264IlefsTer12 | |
| ENST00000278616.8:c.790del | ENSP00000278616.4:p.Tyr264IlefsTer12 | |
| ENST00000452508.6:c.790del | ENSP00000388058.2:p.Tyr264IlefsTer12 | |
| ENST00000527805.5:c.790del | ENSP00000435747.1:p.Tyr264IlefsTer12 | |
| NM_000051.3:c.790del , LRG_135t1:c.790del | NP_000042.3:p.Tyr264IlefsTer12 | |
| XM_005271561.3:c.790del | XP_005271618.2:p.Tyr264IlefsTer12 | |
| XM_005271562.3:c.790del | XP_005271619.2:p.Tyr264IlefsTer12 | |
| XM_006718843.2:c.790del | XP_006718906.1:p.Tyr264IlefsTer12 | |
| XM_011542840.1:c.790del | XP_011541142.1:p.Tyr264IlefsTer12 | |
| XM_011542841.1:c.790del | XP_011541143.1:p.Tyr264IlefsTer12 | |
| XM_011542842.1:c.625del | XP_011541144.1:p.Tyr209IlefsTer12 | |
| XM_011542843.1:c.790del | XP_011541145.1:p.Tyr264IlefsTer12 | |
| XM_011542844.1:c.-255del | XP_011541146.1:n.-255del | |
| XM_011542846.1:c.790del | XP_011541148.1:p.Tyr264IlefsTer12 | |
| NM_001351834.1:c.790del | NP_001338763.1:p.Tyr264IlefsTer12 | |
| XM_005271562.5:c.790del | XP_005271619.2:p.Tyr264IlefsTer12 | |
| XM_006718843.4:c.790del | XP_006718906.1:p.Tyr264IlefsTer12 | |
| XM_011542840.3:c.790del | XP_011541142.1:p.Tyr264IlefsTer12 | |
| XM_011542842.3:c.625del | XP_011541144.1:p.Tyr209IlefsTer12 | |
| XM_011542843.2:c.790del | XP_011541145.1:p.Tyr264IlefsTer12 | |
| XM_011542844.3:c.-255del | XP_011541146.1:n.-255del | |
| XM_017017789.2:c.790del | XP_016873278.1:p.Tyr264IlefsTer12 | |
| XM_017017790.2:c.790del | XP_016873279.1:p.Tyr264IlefsTer12 | |
| XM_017017791.1:c.790del | XP_016873280.1:p.Tyr264IlefsTer12 | |
| XM_017017792.2:c.790del | XP_016873281.1:p.Tyr264IlefsTer12 | |
| XR_002957150.1:n.1523del | ||
| NM_001351834.2:c.790del | NP_001338763.1:p.Tyr264IlefsTer12 | |
| NM_000051.4:c.790del MANE Select | NP_000042.3:p.Tyr264IlefsTer12 |