HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884715_149884717delinsCTA , CM000663.2:g.149884715_149884717delinsCTA | GRCh38 |
NC_000001.10:g.149856265_149856267delinsCTA , CM000663.1:g.149856265_149856267delinsCTA | GRCh37 |
NC_000001.9:g.148122889_148122891delinsCTA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369155.4:c.*1543_*1545delinsTAG MANE Select | ENSP00000358151.2:n.*1543_*1545delinsTAG | |
ENST00000369155.3:c.*1543_*1545delinsTAG | ENSP00000358151.2:n.*1543_*1545delinsTAG | |
ENST00000369160.3:c.377+1547_377+1549delinsTAG | ENSP00000375736.2:n.377+1547_377+1549deli... | |
NM_003528.2:c.*1543_*1545delinsTAG | NP_003519.1:n.*1543_*1545delinsTAG | |
NM_003528.3:c.*1543_*1545delinsTAG MANE Select | NP_003519.1:n.*1543_*1545delinsTAG |