Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70175944_70175946del , CM000679.2:g.70175944_70175946del | GRCh38 |
| NC_000017.10:g.68172085_68172087del , CM000679.1:g.68172085_68172087del | GRCh37 |
| NC_000017.9:g.65683680_65683682del | NCBI36 |
| NG_008798.1:g.11410_11412del , LRG_328:g.11410_11412del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243457.4:c.905_907del MANE Select | ENSP00000243457.2:p.Val302del | |
| ENST00000243457.3:c.905_907del | ENSP00000243457.2:p.Val302del | |
| ENST00000535240.1:c.905_907del | ENSP00000441848.1:p.Val302del | |
| NM_000891.2:c.905_907del , LRG_328t1:c.905_907del | NP_000882.1:p.Val302del | |
| XM_011524779.1:c.905_907del | XP_011523081.1:p.Val302del | |
| NM_000891.3:c.905_907del MANE Select | NP_000882.1:p.Val302del |