Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73323716del , CM000677.2:g.73323716del | GRCh38 |
| NC_000015.9:g.73616057del , CM000677.1:g.73616057del | GRCh37 |
| NC_000015.8:g.71403110del | NCBI36 |
| NG_009063.1:g.50549del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.2377del MANE Select | ENSP00000261917.3:p.Ile793Ter | |
| ENST00000261917.3:c.2377del | ENSP00000261917.3:p.Ile793Ter | |
| NM_005477.2:c.2377del | NP_005468.1:p.Ile793Ter | |
| XM_011521148.1:c.1159del | XP_011519450.1:p.Ile387Ter | |
| XM_011521148.2:c.1159del | XP_011519450.1:p.Ile387Ter | |
| NM_005477.3:c.2377del MANE Select | NP_005468.1:p.Ile793Ter |