HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58782738_58782749del , CM000663.2:g.58782738_58782749del | GRCh38 |
NC_000001.10:g.59248410_59248421del , CM000663.1:g.59248410_59248421del | GRCh37 |
NC_000001.9:g.59020998_59021009del | NCBI36 |
NG_047027.1:g.6375_6386del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000710273.1:c.398_409del | ENSP00000518166.1:p.Ala133_Phe136del | |
ENST00000371222.4:c.332_343del MANE Select | ENSP00000360266.2:p.Ala111_Phe114del | |
ENST00000678696.1:c.332_343del | ENSP00000503132.1:p.Ala111_Phe114del | |
ENST00000371222.3:c.332_343del | ENSP00000360266.2:p.Ala111_Phe114del | |
NM_002228.3:c.332_343del | NP_002219.1:p.Ala111_Phe114del | |
NM_002228.4:c.332_343del MANE Select | NP_002219.1:p.Ala111_Phe114del |