HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58782634_58782654del , CM000663.2:g.58782634_58782654del | GRCh38 |
NC_000001.10:g.59248306_59248326del , CM000663.1:g.59248306_59248326del | GRCh37 |
NC_000001.9:g.59020894_59020914del | NCBI36 |
NG_047027.1:g.6462_6482del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000710273.1:c.485_505del | ENSP00000518166.1:p.Ala162_Ala168del | |
ENST00000371222.4:c.419_439del MANE Select | ENSP00000360266.2:p.Ala140_Ala146del | |
ENST00000678696.1:c.419_439del | ENSP00000503132.1:p.Ala140_Ala146del | |
ENST00000371222.3:c.419_439del | ENSP00000360266.2:p.Ala140_Ala146del | |
NM_002228.3:c.419_439del | NP_002219.1:p.Ala140_Ala146del | |
NM_002228.4:c.419_439del MANE Select | NP_002219.1:p.Ala140_Ala146del |