HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7455997del , CM000679.2:g.7455997del | GRCh38 |
NC_000017.10:g.7359316del , CM000679.1:g.7359316del | GRCh37 |
NC_000017.9:g.7300040del | NCBI36 |
NG_008026.1:g.15911del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000306071.7:c.1365+56del MANE Select | ENSP00000304290.2:n.1365+56del | |
ENST00000306071.6:c.1365+56del | ENSP00000304290.2:n.1365+56del | |
ENST00000536404.6:c.1149+56del | ENSP00000439209.2:n.1149+56del | |
ENST00000575379.1:c.-28+56del | ENSP00000461751.1:n.-28+56del | |
ENST00000576360.1:c.1002+56del | ENSP00000459092.1:n.1002+56del | |
NM_000747.2:c.1365+56del | NP_000738.2:n.1365+56del | |
NM_000747.3:c.1365+56del MANE Select | NP_000738.2:n.1365+56del |