HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47332513del , CM000673.2:g.47332513del | GRCh38 |
NC_000011.9:g.47354064del , CM000673.1:g.47354064del | GRCh37 |
NC_000011.8:g.47310640del | NCBI36 |
NG_007667.1:g.25193del , LRG_386:g.25193del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000545968.6:c.3627+56del MANE Select | ENSP00000442795.1:n.3627+56del | |
ENST00000256993.8:c.3627+56del | ENSP00000256993.5:n.3627+56del | |
ENST00000399249.6:c.3627+56del | ENSP00000382193.2:n.3627+56del | |
ENST00000545968.5:c.3627+56del | ENSP00000442795.1:n.3627+56del | |
NM_000256.3:c.3627+56del , LRG_386t1:c.3627+56del MANE Select | NP_000247.2:n.3627+56del | |
XM_011520117.1:c.3609+56del | XP_011518419.1:n.3609+56del | |
XM_011520118.1:c.3546+56del | XP_011518420.1:n.3546+56del |