HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58782738_58782749dup , CM000663.2:g.58782738_58782749dup | GRCh38 |
NC_000001.10:g.59248410_59248421dup , CM000663.1:g.59248410_59248421dup | GRCh37 |
NC_000001.9:g.59020998_59021009dup | NCBI36 |
NG_047027.1:g.6375_6386dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000710273.1:c.398_409dup | ENSP00000518166.1:p.Phe136_Val137insAlaGluGlyPhe | |
ENST00000371222.4:c.332_343dup MANE Select | ENSP00000360266.2:p.Phe114_Val115insAlaGluGlyPhe | |
ENST00000678696.1:c.332_343dup | ENSP00000503132.1:p.Phe114_Val115insAlaGluGlyPhe | |
ENST00000371222.3:c.332_343dup | ENSP00000360266.2:p.Phe114_Val115insAlaGluGlyPhe | |
NM_002228.3:c.332_343dup | NP_002219.1:p.Phe114_Val115insAlaGluGlyPhe | |
NM_002228.4:c.332_343dup MANE Select | NP_002219.1:p.Phe114_Val115insAlaGluGlyPhe |