Canonical Allele Identifier: CA2276860659
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223946G= , CM000679.2:g.78223946G= GRCh38
NC_000017.10:g.76220027G= , CM000679.1:g.76220027G= GRCh37
NC_000017.9:g.73731622G= NCBI36
NG_029069.1:g.14751G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*392G= MANE Select ENSP00000324180.4:n.*392G=
ENST00000301633.8:c.*392G= ENSP00000301633.3:n.*392G=
ENST00000350051.7:c.*392G= ENSP00000324180.4:n.*392G=
ENST00000374948.6:c.*289G= ENSP00000364086.1:n.*289G=
NM_001012270.1:c.*289G= NP_001012270.1:n.*289G=
NM_001012271.1:c.*392G= NP_001012271.1:n.*392G=
NM_001168.2:c.*392G= NP_001159.2:n.*392G=
XR_243654.3:n.1023G=
XR_934452.1:n.1092G=
XR_243654.5:n.1023G=
XR_934452.3:n.1092G=
NM_001168.3:c.*392G= MANE Select NP_001159.2:n.*392G=
NM_001012270.2:c.*289G= NP_001012270.1:n.*289G=
NM_001012271.2:c.*392G= NP_001012271.1:n.*392G=