Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429953_68429957del , CM000663.2:g.68429953_68429957del | GRCh38 |
| NC_000001.10:g.68895636_68895640del , CM000663.1:g.68895636_68895640del | GRCh37 |
| NC_000001.9:g.68668224_68668228del | NCBI36 |
| NG_008472.1:g.25003_25007del | |
| NG_008472.2:g.25003_25007del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1451-30_1451-26del MANE Select | ENSP00000262340.5:n.1451-30_1451-26del | |
| ENST00000262340.5:c.1451-30_1451-26del | ENSP00000262340.5:n.1451-30_1451-26del | |
| NM_000329.2:c.1451-30_1451-26del | NP_000320.1:n.1451-30_1451-26del | |
| XM_017002027.1:c.1175-30_1175-26del | XP_016857516.1:n.1175-30_1175-26del | |
| NM_000329.3:c.1451-30_1451-26del MANE Select | NP_000320.1:n.1451-30_1451-26del |