Linked Data
ClinVar Variation Id:
232133
dbSNP Id:
rs876659575
gnomAD v2:
11-108124560-AAAG-A
gnomAD v3:
11-108253833-AAAG-A
gnomAD v4:
11-108253833-AAAG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108253839_108253841del , CM000673.2:g.108253839_108253841del | GRCh38 |
| NC_000011.9:g.108124566_108124568del , CM000673.1:g.108124566_108124568del | GRCh37 |
| NC_000011.8:g.107629776_107629778del | NCBI36 |
| NG_009830.1:g.36008_36010del , LRG_135:g.36008_36010del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.1924_1926del | ENSP00000388058.2:p.Glu642del | |
| ENST00000713593.1:c.*1395_*1397del | ENSP00000518889.1:n.*1395_*1397del | |
| ENST00000278616.9:c.1924_1926del | ENSP00000278616.4:p.Glu642del | |
| ENST00000682516.1:n.2058_2060del | ||
| ENST00000683174.1:n.2074_2076del | ||
| ENST00000683605.1:n.1419_1421del | ||
| ENST00000684037.1:c.*859_*861del | ENSP00000508245.1:n.*859_*861del | |
| ENST00000684061.1:n.2058_2060del | ||
| ENST00000527805.6:c.1924_1926del | ENSP00000435747.2:p.Glu642del | |
| ENST00000675595.1:c.1759_1761del | ENSP00000502563.1:p.Glu587del | |
| ENST00000675843.1:c.1924_1926del MANE Select | ENSP00000501606.1:p.Glu642del | |
| ENST00000278616.8:c.1924_1926del | ENSP00000278616.4:p.Glu642del | |
| ENST00000452508.6:c.1924_1926del | ENSP00000388058.2:p.Glu642del | |
| ENST00000525012.5:n.101_103del | ||
| ENST00000527805.5:c.1924_1926del | ENSP00000435747.1:p.Glu642del | |
| ENST00000533526.1:n.93-16_93-14del | ||
| NM_000051.3:c.1924_1926del , LRG_135t1:c.1924_1926del | NP_000042.3:p.Glu642del | |
| XM_005271561.3:c.1924_1926del | XP_005271618.2:p.Glu642del | |
| XM_005271562.3:c.1924_1926del | XP_005271619.2:p.Glu642del | |
| XM_006718843.2:c.1924_1926del | XP_006718906.1:p.Glu642del | |
| XM_011542840.1:c.1924_1926del | XP_011541142.1:p.Glu642del | |
| XM_011542841.1:c.1924_1926del | XP_011541143.1:p.Glu642del | |
| XM_011542842.1:c.1759_1761del | XP_011541144.1:p.Glu587del | |
| XM_011542843.1:c.1924_1926del | XP_011541145.1:p.Glu642del | |
| XM_011542844.1:c.880_882del | XP_011541146.1:p.Glu294del | |
| XM_011542845.1:c.616_618del | XP_011541147.1:p.Glu206del | |
| XM_011542846.1:c.1924_1926del | XP_011541148.1:p.Glu642del | |
| NM_001351834.1:c.1924_1926del | NP_001338763.1:p.Glu642del | |
| XM_005271562.5:c.1924_1926del | XP_005271619.2:p.Glu642del | |
| XM_006718843.4:c.1924_1926del | XP_006718906.1:p.Glu642del | |
| XM_011542840.3:c.1924_1926del | XP_011541142.1:p.Glu642del | |
| XM_011542842.3:c.1759_1761del | XP_011541144.1:p.Glu587del | |
| XM_011542843.2:c.1924_1926del | XP_011541145.1:p.Glu642del | |
| XM_011542844.3:c.880_882del | XP_011541146.1:p.Glu294del | |
| XM_011542845.2:c.616_618del | XP_011541147.1:p.Glu206del | |
| XM_017017789.2:c.1924_1926del | XP_016873278.1:p.Glu642del | |
| XM_017017790.2:c.1924_1926del | XP_016873279.1:p.Glu642del | |
| XM_017017791.1:c.1924_1926del | XP_016873280.1:p.Glu642del | |
| XM_017017792.2:c.1924_1926del | XP_016873281.1:p.Glu642del | |
| XR_002957150.1:n.2657_2659del | ||
| NM_001351834.2:c.1924_1926del | NP_001338763.1:p.Glu642del | |
| NM_000051.4:c.1924_1926del MANE Select | NP_000042.3:p.Glu642del |