Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429976_68429978del , CM000663.2:g.68429976_68429978del | GRCh38 |
| NC_000001.10:g.68895659_68895661del , CM000663.1:g.68895659_68895661del | GRCh37 |
| NC_000001.9:g.68668247_68668249del | NCBI36 |
| NG_008472.1:g.24982_24984del | |
| NG_008472.2:g.24982_24984del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1451-51_1451-49del MANE Select | ENSP00000262340.5:n.1451-51_1451-49del | |
| ENST00000262340.5:c.1451-51_1451-49del | ENSP00000262340.5:n.1451-51_1451-49del | |
| NM_000329.2:c.1451-51_1451-49del | NP_000320.1:n.1451-51_1451-49del | |
| XM_017002027.1:c.1175-51_1175-49del | XP_016857516.1:n.1175-51_1175-49del | |
| NM_000329.3:c.1451-51_1451-49del MANE Select | NP_000320.1:n.1451-51_1451-49del |