HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44305209_44305220del , CM000667.2:g.44305209_44305220del | GRCh38 |
NC_000005.9:g.44305311_44305322del , CM000667.1:g.44305311_44305322del | GRCh37 |
NC_000005.8:g.44341068_44341079del | NCBI36 |
NG_011446.1:g.88463_88474del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.430-28_430-17del MANE Select | ENSP00000264664.4:n.430-28_430-17del | |
ENST00000264664.4:c.430-28_430-17del | ENSP00000264664.4:n.430-28_430-17del | |
NM_004465.1:c.430-28_430-17del | NP_004456.1:n.430-28_430-17del | |
XM_005248264.2:c.430-28_430-17del | XP_005248321.1:n.430-28_430-17del | |
XM_005248264.4:c.430-28_430-17del | XP_005248321.1:n.430-28_430-17del | |
NM_004465.2:c.430-28_430-17del MANE Select | NP_004456.1:n.430-28_430-17del |