Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67054020del , CM000663.2:g.67054020del | GRCh38 |
| NC_000001.10:g.67519703del , CM000663.1:g.67519703del | GRCh37 |
| NC_000001.9:g.67292291del | NCBI36 |
| NG_012933.1:g.5379del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000235345.6:c.-6del MANE Select | ENSP00000235345.5:n.-6del | |
| ENST00000235345.5:c.-6del | ENSP00000235345.5:n.-6del | |
| NM_015139.2:c.-6del | NP_055954.1:n.-6del | |
| XM_006710478.1:c.-6del | XP_006710541.1:n.-6del | |
| XM_011541070.1:c.-6del | XP_011539372.1:n.-6del | |
| XM_006710478.2:c.-6del | XP_006710541.1:n.-6del | |
| XM_011541070.2:c.-6del | XP_011539372.1:n.-6del | |
| XR_001737057.2:n.405del | ||
| XR_001737058.2:n.398del | ||
| NM_015139.3:c.-6del MANE Select | NP_055954.1:n.-6del |