HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49828959_49828964del , CM000665.2:g.49828959_49828964del | GRCh38 |
NC_000003.11:g.49866392_49866397del , CM000665.1:g.49866392_49866397del | GRCh37 |
NC_000003.10:g.49841396_49841401del | NCBI36 |
NG_046695.1:g.32596_32601del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000331456.7:c.*139_*144del MANE Select | ENSP00000328203.2:n.*139_*144del | |
ENST00000331456.6:c.*139_*144del | ENSP00000328203.2:n.*139_*144del | |
ENST00000491060.1:n.703_708del | ||
NM_005879.2:c.*139_*144del | NP_005870.2:n.*139_*144del | |
XM_011533264.1:c.*139_*144del | XP_011531566.1:n.*139_*144del | |
XM_017005526.1:c.*139_*144del | XP_016861015.1:n.*139_*144del | |
XR_001739979.1:n.1753_1758del | ||
NM_005879.3:c.*139_*144del MANE Select | NP_005870.2:n.*139_*144del |