HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154091_55154092delinsGC , CM000681.2:g.55154091_55154092delinsGC | GRCh38 |
NC_000019.9:g.55665459_55665460delinsGC , CM000681.1:g.55665459_55665460delinsGC | GRCh37 |
NC_000019.8:g.60357271_60357272delinsGC | NCBI36 |
NG_007866.2:g.8641_8642delinsGC , LRG_432:g.8641_8642delinsGC | |
NG_011829.2:g.147_148delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.487_488delinsGC MANE Select | ENSP00000341838.5:p.Ala163= | |
ENST00000665070.1:c.520_521delinsGC | ENSP00000499482.1:p.Ala174= | |
ENST00000344887.9:c.487_488delinsGC | ENSP00000341838.5:p.Ala163= | |
ENST00000585806.5:n.486_487delinsGC | ||
ENST00000588882.1:c.412_413delinsGC | ENSP00000466729.1:p.Ala138= | |
ENST00000589864.1:n.315_316delinsGC | ||
NM_000363.4:c.487_488delinsGC , LRG_432t1:c.487_488delinsGC | NP_000354.4:p.Ala163= | |
NM_000363.5:c.487_488delinsGC MANE Select | NP_000354.4:p.Ala163= |