HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49828970_49828975del , CM000665.2:g.49828970_49828975del | GRCh38 |
NC_000003.11:g.49866403_49866408del , CM000665.1:g.49866403_49866408del | GRCh37 |
NC_000003.10:g.49841407_49841412del | NCBI36 |
NG_046695.1:g.32591_32596del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000331456.7:c.*134_*139del MANE Select | ENSP00000328203.2:n.*134_*139del | |
ENST00000331456.6:c.*134_*139del | ENSP00000328203.2:n.*134_*139del | |
ENST00000491060.1:n.698_703del | ||
NM_005879.2:c.*134_*139del | NP_005870.2:n.*134_*139del | |
XM_011533264.1:c.*134_*139del | XP_011531566.1:n.*134_*139del | |
XM_017005526.1:c.*134_*139del | XP_016861015.1:n.*134_*139del | |
XR_001739979.1:n.1748_1753del | ||
NM_005879.3:c.*134_*139del MANE Select | NP_005870.2:n.*134_*139del |