Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94042962_94042971del , CM000663.2:g.94042962_94042971del | GRCh38 |
| NC_000001.10:g.94508518_94508527del , CM000663.1:g.94508518_94508527del | GRCh37 |
| NC_000001.9:g.94281106_94281115del | NCBI36 |
| NG_009073.1:g.83179_83188del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.3191-73_3191-64del MANE Select | ENSP00000359245.3:n.3191-73_3191-64del | |
| ENST00000370225.3:c.3191-73_3191-64del | ENSP00000359245.3:n.3191-73_3191-64del | |
| ENST00000536513.5:c.-64-2882_-64-2873del | ENSP00000439707.2:n.-64-2882_-64-2873del | |
| NM_000350.2:c.3191-73_3191-64del | NP_000341.2:n.3191-73_3191-64del | |
| NM_000350.3:c.3191-73_3191-64del MANE Select | NP_000341.2:n.3191-73_3191-64del |