HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44305749del , CM000667.2:g.44305749del | GRCh38 |
NC_000005.9:g.44305851del , CM000667.1:g.44305851del | GRCh37 |
NC_000005.8:g.44341608del | NCBI36 |
NG_011446.1:g.87934del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.430-557del MANE Select | ENSP00000264664.4:n.430-557del | |
ENST00000264664.4:c.430-557del | ENSP00000264664.4:n.430-557del | |
NM_004465.1:c.430-557del | NP_004456.1:n.430-557del | |
XM_005248264.2:c.430-557del | XP_005248321.1:n.430-557del | |
XM_005248264.4:c.430-557del | XP_005248321.1:n.430-557del | |
NM_004465.2:c.430-557del MANE Select | NP_004456.1:n.430-557del |