Linked Data
gnomAD v2:
11-134132554-C-CG
gnomAD v4:
11-134262660-C-CG
MyVariant Identifiers:
chr11:g.134132554_134132555insG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.134262665dup , CM000673.2:g.134262665dup | GRCh38 |
| NC_000011.9:g.134132559dup , CM000673.1:g.134132559dup | GRCh37 |
| NC_000011.8:g.133637769dup | NCBI36 |
| NG_015842.1:g.14126dup , LRG_448:g.14126dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281182.9:c.1195+43dup MANE Select | ENSP00000281182.5:n.1195+43dup | |
| ENST00000281182.8:c.1195+43dup | ENSP00000281182.4:n.1195+43dup | |
| ENST00000374752.6:c.814+43dup | ENSP00000363884.4:n.814+43dup | |
| ENST00000524502.2:n.195+43dup | ||
| ENST00000526026.5:c.*884+43dup | ENSP00000431532.1:n.*884+43dup | |
| ENST00000531338.5:n.1482dup | ||
| ENST00000533387.5:n.2254+43dup | ||
| NM_014384.2:c.1195+43dup , LRG_448t1:c.1195+43dup | NP_055199.1:n.1195+43dup | |
| XM_005271501.2:c.1195+43dup | XP_005271558.1:n.1195+43dup | |
| XM_011542750.1:c.1195+43dup | XP_011541052.1:n.1195+43dup | |
| XR_947819.1:n.1259+43dup | ||
| XR_947820.1:n.1690dup | ||
| XR_947822.1:n.1089+43dup | ||
| XR_947823.1:n.1245+43dup | ||
| XM_005271505.4:c.*1460+43dup | XP_005271562.1:n.*1460+43dup | |
| XM_011542750.3:c.1195+43dup | XP_011541052.1:n.1195+43dup | |
| XM_017017542.2:c.1195+43dup | XP_016873031.1:n.1195+43dup | |
| XM_017017543.2:c.1195+43dup | XP_016873032.1:n.1195+43dup | |
| XM_017017544.2:c.*164+43dup | XP_016873033.1:n.*164+43dup | |
| XM_017017545.2:c.*450dup | XP_016873034.1:n.*450dup | |
| XM_017017546.2:c.901+43dup | XP_016873035.1:n.901+43dup | |
| XM_017017547.2:c.901+43dup | XP_016873036.1:n.901+43dup | |
| XM_017017548.2:c.*1831+43dup | XP_016873037.1:n.*1831+43dup | |
| XM_017017549.2:c.*1605+43dup | XP_016873038.1:n.*1605+43dup | |
| XM_024448437.1:c.*385dup | XP_024304205.1:n.*385dup | |
| XM_024448438.1:c.814+43dup | XP_024304206.1:n.814+43dup | |
| NM_014384.3:c.1195+43dup MANE Select | NP_055199.1:n.1195+43dup |