Canonical Allele Identifier: CA2276860614
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223792T= , CM000679.2:g.78223792T= GRCh38
NC_000017.10:g.76219873T= , CM000679.1:g.76219873T= GRCh37
NC_000017.9:g.73731468T= NCBI36
NG_029069.1:g.14597T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*238T= MANE Select ENSP00000324180.4:n.*238T=
ENST00000301633.8:c.*238T= ENSP00000301633.3:n.*238T=
ENST00000350051.7:c.*238T= ENSP00000324180.4:n.*238T=
ENST00000374948.6:c.*135T= ENSP00000364086.1:n.*135T=
ENST00000589892.1:n.683T=
NM_001012270.1:c.*135T= NP_001012270.1:n.*135T=
NM_001012271.1:c.*238T= NP_001012271.1:n.*238T=
NM_001168.2:c.*238T= NP_001159.2:n.*238T=
XR_243654.3:n.869T=
XR_934452.1:n.938T=
XR_243654.5:n.869T=
XR_934452.3:n.938T=
NM_001168.3:c.*238T= MANE Select NP_001159.2:n.*238T=
NM_001012270.2:c.*135T= NP_001012270.1:n.*135T=
NM_001012271.2:c.*238T= NP_001012271.1:n.*238T=