Canonical Allele Identifier: CA2276860433

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223301C= , CM000679.2:g.78223301C=	GRCh38
NC_000017.10:g.76219382C= , CM000679.1:g.76219382C=	GRCh37
NC_000017.9:g.73730977C=	NCBI36
NG_029069.1:g.14106C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.340-164C= MANE Select	ENSP00000324180.4:n.340-164C=
ENST00000301633.8:c.409-164C=	ENSP00000301633.3:n.409-164C=
ENST00000350051.7:c.340-164C=	ENSP00000324180.4:n.340-164C=
ENST00000374948.6:c.222-164C=	ENSP00000364086.1:n.222-164C=
ENST00000589892.1:n.356-164C=
ENST00000590925.6:c.*142-164C=	ENSP00000467336.1:n.*142-164C=
NM_001012270.1:c.222-164C=	NP_001012270.1:n.222-164C=
NM_001012271.1:c.409-164C=	NP_001012271.1:n.409-164C=
NM_001168.2:c.340-164C=	NP_001159.2:n.340-164C=
XR_243654.3:n.542-164C=
XR_934452.1:n.611-164C=
XR_243654.5:n.542-164C=
XR_934452.3:n.611-164C=
NM_001168.3:c.340-164C= MANE Select	NP_001159.2:n.340-164C=
NM_001012270.2:c.222-164C=	NP_001012270.1:n.222-164C=
NM_001012271.2:c.409-164C=	NP_001012271.1:n.409-164C=