HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154643del , CM000681.2:g.55154643del | GRCh38 |
NC_000019.9:g.55666011del , CM000681.1:g.55666011del | GRCh37 |
NC_000019.8:g.60357823del | NCBI36 |
NG_007866.2:g.8092del , LRG_432:g.8092del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.372+100del MANE Select | ENSP00000341838.5:n.372+100del | |
ENST00000665070.1:c.405+67del | ENSP00000499482.1:n.405+67del | |
ENST00000344887.9:c.372+100del | ENSP00000341838.5:n.372+100del | |
ENST00000585806.5:n.371+100del | ||
ENST00000586669.5:n.380+100del | ||
ENST00000587176.5:n.656del | ||
ENST00000588882.1:c.297+100del | ENSP00000466729.1:n.297+100del | |
NM_000363.4:c.372+100del , LRG_432t1:c.372+100del | NP_000354.4:n.372+100del | |
NM_000363.5:c.372+100del MANE Select | NP_000354.4:n.372+100del |