HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4934095_4934100del , CM000679.2:g.4934095_4934100del | GRCh38 |
NC_000017.10:g.4837390_4837395del , CM000679.1:g.4837390_4837395del | GRCh37 |
NC_000017.9:g.4778131_4778136del | NCBI36 |
NG_008767.2:g.6801_6806del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000329125.6:c.1491_1496del (GP1BA) MANE Select | ENSP00000329380.5:p.Glu497_Leu498del | |
ENST00000649830.1:c.-888+245_-888+250del (CHRNE) | ENSP00000496907.1:n.-888+245_-888+250del | |
ENST00000329125.5:c.1491_1496del (GP1BA) | ENSP00000329380.5:p.Glu497_Leu498del | |
ENST00000611961.1:c.1413_1418del (GP1BA) | ENSP00000484439.1:p.Glu471_Leu472del | |
NM_000173.6:c.1491_1496del (GP1BA) | NP_000164.5:p.Glu497_Leu498del | |
NM_000173.7:c.1491_1496del (GP1BA) MANE Select | NP_000164.5:p.Glu497_Leu498del |