Canonical Allele Identifier: CA2276860792
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224136C= , CM000679.2:g.78224136C= GRCh38
NC_000017.10:g.76220217C= , CM000679.1:g.76220217C= GRCh37
NC_000017.9:g.73731812C= NCBI36
NG_029069.1:g.14941C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*582C= MANE Select ENSP00000324180.4:n.*582C=
ENST00000301633.8:c.*582C= ENSP00000301633.3:n.*582C=
ENST00000350051.7:c.*582C= ENSP00000324180.4:n.*582C=
ENST00000374948.6:c.*479C= ENSP00000364086.1:n.*479C=
NM_001012270.1:c.*479C= NP_001012270.1:n.*479C=
NM_001012271.1:c.*582C= NP_001012271.1:n.*582C=
NM_001168.2:c.*582C= NP_001159.2:n.*582C=
XR_243654.3:n.1213C=
XR_934452.1:n.1282C=
XR_243654.5:n.1213C=
XR_934452.3:n.1282C=
NM_001168.3:c.*582C= MANE Select NP_001159.2:n.*582C=
NM_001012270.2:c.*479C= NP_001012270.1:n.*479C=
NM_001012271.2:c.*582C= NP_001012271.1:n.*582C=