HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17356173del , CM000663.2:g.17356173del | GRCh38 |
NC_000001.10:g.17682668del , CM000663.1:g.17682668del | GRCh37 |
NC_000001.9:g.17555255del | NCBI36 |
NG_023261.2:g.52984del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375448.4:c.1455+46del MANE Select | ENSP00000364597.4:n.1455+46del | |
ENST00000467001.1:n.356+46del | ||
ENST00000487048.5:n.422+46del | ||
NM_012387.2:c.1455+46del | NP_036519.2:n.1455+46del | |
XM_011541150.1:c.1269+46del | XP_011539452.1:n.1269+46del | |
XM_011541151.1:c.1156-184del | XP_011539453.1:n.1156-184del | |
XM_011541152.1:c.918+46del | XP_011539454.1:n.918+46del | |
XM_011541157.1:c.564+46del | XP_011539459.1:n.564+46del | |
NM_012387.3:c.1455+46del MANE Select | NP_036519.2:n.1455+46del |