HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154097_55154098delinsGC , CM000681.2:g.55154097_55154098delinsGC | GRCh38 |
NC_000019.9:g.55665465_55665466delinsGC , CM000681.1:g.55665465_55665466delinsGC | GRCh37 |
NC_000019.8:g.60357277_60357278delinsGC | NCBI36 |
NG_007866.2:g.8635_8636delinsGC , LRG_432:g.8635_8636delinsGC | |
NG_011829.2:g.141_142delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.481_482delinsGC MANE Select | ENSP00000341838.5:p.Ala161= | |
ENST00000665070.1:c.514_515delinsGC | ENSP00000499482.1:p.Ala172= | |
ENST00000344887.9:c.481_482delinsGC | ENSP00000341838.5:p.Ala161= | |
ENST00000585806.5:n.480_481delinsGC | ||
ENST00000588882.1:c.406_407delinsGC | ENSP00000466729.1:p.Ala136= | |
ENST00000589864.1:n.309_310delinsGC | ||
NM_000363.4:c.481_482delinsGC , LRG_432t1:c.481_482delinsGC | NP_000354.4:p.Ala161= | |
NM_000363.5:c.481_482delinsGC MANE Select | NP_000354.4:p.Ala161= |