Linked Data
ClinVar Variation Id:
551735
dbSNP Id:
rs1555096057
MyVariant Identifiers:
chr11:g.108287701_108287702del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108287701_108287702del , CM000673.2:g.108287701_108287702del | GRCh38 |
| NC_000011.9:g.108158428_108158429del , CM000673.1:g.108158428_108158429del | GRCh37 |
| NC_000011.8:g.107663638_107663639del | NCBI36 |
| NG_009830.1:g.69870_69871del , LRG_135:g.69870_69871del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.4095_4096del | ENSP00000388058.2:p.Cys1366Ter | |
| ENST00000713593.1:c.*3566_*3567del | ENSP00000518889.1:n.*3566_*3567del | |
| ENST00000278616.9:c.4095_4096del | ENSP00000278616.4:p.Cys1366Ter | |
| ENST00000533733.6:n.1358_1359del | ||
| ENST00000683174.1:n.4245_4246del | ||
| ENST00000527805.6:c.4095_4096del | ENSP00000435747.2:p.Cys1366Ter | |
| ENST00000675595.1:c.3930_3931del | ENSP00000502563.1:p.Cys1311Ter | |
| ENST00000675843.1:c.4095_4096del MANE Select | ENSP00000501606.1:p.Cys1366Ter | |
| ENST00000278616.8:c.4095_4096del | ENSP00000278616.4:p.Cys1366Ter | |
| ENST00000452508.6:c.4095_4096del | ENSP00000388058.2:p.Cys1366Ter | |
| ENST00000524792.5:n.310_311del | ||
| ENST00000527805.5:c.4095_4096del | ENSP00000435747.1:p.Cys1366Ter | |
| ENST00000531525.2:c.102_103del | ENSP00000434327.2:p.Cys35Ter | |
| ENST00000533733.5:n.524_525del | ||
| NM_000051.3:c.4095_4096del , LRG_135t1:c.4095_4096del | NP_000042.3:p.Cys1366Ter | |
| XM_005271561.3:c.4095_4096del | XP_005271618.2:p.Cys1366Ter | |
| XM_005271562.3:c.4095_4096del | XP_005271619.2:p.Cys1366Ter | |
| XM_006718843.2:c.4095_4096del | XP_006718906.1:p.Cys1366Ter | |
| XM_006718845.1:c.51_52del | XP_006718908.1:p.Cys18Ter | |
| XM_011542840.1:c.4095_4096del | XP_011541142.1:p.Cys1366Ter | |
| XM_011542841.1:c.4095_4096del | XP_011541143.1:p.Cys1366Ter | |
| XM_011542842.1:c.3930_3931del | XP_011541144.1:p.Cys1311Ter | |
| XM_011542843.1:c.4095_4096del | XP_011541145.1:p.Cys1366Ter | |
| XM_011542844.1:c.3051_3052del | XP_011541146.1:p.Cys1018Ter | |
| XM_011542845.1:c.2787_2788del | XP_011541147.1:p.Cys930Ter | |
| XM_011542846.1:c.4095_4096del | XP_011541148.1:p.Cys1366Ter | |
| NM_001351834.1:c.4095_4096del | NP_001338763.1:p.Cys1366Ter | |
| XM_005271562.5:c.4095_4096del | XP_005271619.2:p.Cys1366Ter | |
| XM_006718843.4:c.4095_4096del | XP_006718906.1:p.Cys1366Ter | |
| XM_006718845.2:c.51_52del | XP_006718908.1:p.Cys18Ter | |
| XM_011542840.3:c.4095_4096del | XP_011541142.1:p.Cys1366Ter | |
| XM_011542842.3:c.3930_3931del | XP_011541144.1:p.Cys1311Ter | |
| XM_011542843.2:c.4095_4096del | XP_011541145.1:p.Cys1366Ter | |
| XM_011542844.3:c.3051_3052del | XP_011541146.1:p.Cys1018Ter | |
| XM_011542845.2:c.2787_2788del | XP_011541147.1:p.Cys930Ter | |
| XM_017017789.2:c.4095_4096del | XP_016873278.1:p.Cys1366Ter | |
| XM_017017790.2:c.4095_4096del | XP_016873279.1:p.Cys1366Ter | |
| XM_017017791.1:c.4095_4096del | XP_016873280.1:p.Cys1366Ter | |
| XM_017017792.2:c.4095_4096del | XP_016873281.1:p.Cys1366Ter | |
| XR_002957150.1:n.4828_4829del | ||
| NM_001351834.2:c.4095_4096del | NP_001338763.1:p.Cys1366Ter | |
| NM_000051.4:c.4095_4096del MANE Select | NP_000042.3:p.Cys1366Ter |