HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7455785del , CM000679.2:g.7455785del | GRCh38 |
NC_000017.10:g.7359104del , CM000679.1:g.7359104del | GRCh37 |
NC_000017.9:g.7299828del | NCBI36 |
NG_008026.1:g.15699del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000306071.7:c.1218-9del MANE Select | ENSP00000304290.2:n.1218-9del | |
ENST00000306071.6:c.1218-9del | ENSP00000304290.2:n.1218-9del | |
ENST00000536404.6:c.1002-9del | ENSP00000439209.2:n.1002-9del | |
ENST00000570557.5:c.881-9del | ||
ENST00000575379.1:c.-184del | ENSP00000461751.1:n.-184del | |
ENST00000576360.1:c.855-9del | ENSP00000459092.1:n.855-9del | |
NM_000747.2:c.1218-9del | NP_000738.2:n.1218-9del | |
NM_000747.3:c.1218-9del MANE Select | NP_000738.2:n.1218-9del |