Canonical Allele Identifier: CA2276860612

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223790_78223791delinsCT , CM000679.2:g.78223790_78223791delinsCT	GRCh38
NC_000017.10:g.76219871_76219872delinsCT , CM000679.1:g.76219871_76219872delinsCT	GRCh37
NC_000017.9:g.73731466_73731467delinsCT	NCBI36
NG_029069.1:g.14595_14596delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*236_*237delinsCT MANE Select	ENSP00000324180.4:n.*236_*237delinsCT
ENST00000301633.8:c.*236_*237delinsCT	ENSP00000301633.3:n.*236_*237delinsCT
ENST00000350051.7:c.*236_*237delinsCT	ENSP00000324180.4:n.*236_*237delinsCT
ENST00000374948.6:c.*133_*134delinsCT	ENSP00000364086.1:n.*133_*134delinsCT
ENST00000589892.1:n.681_682delinsCT
NM_001012270.1:c.*133_*134delinsCT	NP_001012270.1:n.*133_*134delinsCT
NM_001012271.1:c.*236_*237delinsCT	NP_001012271.1:n.*236_*237delinsCT
NM_001168.2:c.*236_*237delinsCT	NP_001159.2:n.*236_*237delinsCT
XR_243654.3:n.867_868delinsCT
XR_934452.1:n.936_937delinsCT
XR_243654.5:n.867_868delinsCT
XR_934452.3:n.936_937delinsCT
NM_001168.3:c.*236_*237delinsCT MANE Select	NP_001159.2:n.*236_*237delinsCT
NM_001012270.2:c.*133_*134delinsCT	NP_001012270.1:n.*133_*134delinsCT
NM_001012271.2:c.*236_*237delinsCT	NP_001012271.1:n.*236_*237delinsCT