Canonical Allele Identifier: CA401214684
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs1408311951

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223500G>A , CM000679.2:g.78223500G>A GRCh38
NC_000017.10:g.76219581G>A , CM000679.1:g.76219581G>A GRCh37
NC_000017.9:g.73731176G>A NCBI36
NG_029069.1:g.14305G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.375G>A MANE Select ENSP00000324180.4:p.Glu125=
ENST00000301633.8:c.444G>A ENSP00000301633.3:p.Glu148=
ENST00000350051.7:c.375G>A ENSP00000324180.4:p.Glu125=
ENST00000374948.6:c.257G>A ENSP00000364086.1:p.Arg86Lys
ENST00000589892.1:n.391G>A
ENST00000590925.6:c.*177G>A ENSP00000467336.1:n.*177G>A
NM_001012270.1:c.257G>A NP_001012270.1:p.Arg86Lys
NM_001012271.1:c.444G>A NP_001012271.1:p.Glu148=
NM_001168.2:c.375G>A NP_001159.2:p.Glu125=
XR_243654.3:n.577G>A
XR_934452.1:n.646G>A
XR_243654.5:n.577G>A
XR_934452.3:n.646G>A
NM_001168.3:c.375G>A MANE Select NP_001159.2:p.Glu125=
NM_001012270.2:c.257G>A NP_001012270.1:p.Arg86Lys
NM_001012271.2:c.444G>A NP_001012271.1:p.Glu148=