Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8012359_8012363del , CM000679.2:g.8012359_8012363del | GRCh38 |
| NC_000017.10:g.7915677_7915681del , CM000679.1:g.7915677_7915681del | GRCh37 |
| NC_000017.9:g.7856402_7856406del | NCBI36 |
| NG_009092.1:g.14690_14694del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.1956+9_1956+13del MANE Select | ENSP00000254854.4:n.1956+9_1956+13del | |
| ENST00000254854.4:c.1956+9_1956+13del | ENSP00000254854.4:n.1956+9_1956+13del | |
| NM_000180.3:c.1956+9_1956+13del | NP_000171.1:n.1956+9_1956+13del | |
| XM_011523816.1:c.1956+9_1956+13del | XP_011522118.1:n.1956+9_1956+13del | |
| NM_000180.4:c.1956+9_1956+13del MANE Select | NP_000171.1:n.1956+9_1956+13del |