HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44288460_44288463del , CM000683.2:g.44288460_44288463del | GRCh38 |
NC_000021.8:g.45708343_45708346del , CM000683.1:g.45708343_45708346del | GRCh37 |
NC_000021.7:g.44532771_44532774del | NCBI36 |
NG_009556.1:g.7581_7584del , LRG_18:g.7581_7584del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.652+2_652+5del MANE Select | ENSP00000291582.5:n.652+2_652+5del | |
ENST00000291582.5:c.652+2_652+5del | ENSP00000291582.5:n.652+2_652+5del | |
ENST00000527919.5:n.1196+2_1196+5del | ||
ENST00000530812.5:n.1206_1209del | ||
NM_000383.3:c.652+2_652+5del | NP_000374.1:n.652+2_652+5del | |
XM_011529551.1:c.652+2_652+5del | XP_011527853.1:n.652+2_652+5del | |
NM_000383.4:c.652+2_652+5del MANE Select | NP_000374.1:n.652+2_652+5del |