Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.5022530_5022532del , CM000679.2:g.5022530_5022532del | GRCh38 |
| NC_000017.10:g.4925825_4925827del , CM000679.1:g.4925825_4925827del | GRCh37 |
| NC_000017.9:g.4866549_4866551del | NCBI36 |
| NG_034137.1:g.29583_29585del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320785.10:c.2449_2451del MANE Select | ENSP00000320821.5:p.Ser817del | |
| ENST00000320785.9:c.2449_2451del | ENSP00000320821.5:p.Ser817del | |
| NM_006612.5:c.2449_2451del | NP_006603.2:p.Ser817del | |
| XM_005256424.1:c.2449_2451del | XP_005256481.1:p.Ser817del | |
| XM_005256424.2:c.2449_2451del | XP_005256481.1:p.Ser817del | |
| NM_006612.6:c.2449_2451del MANE Select | NP_006603.2:p.Ser817del |