Canonical Allele Identifier: CA2276860583

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223701_78223703delinsCTT , CM000679.2:g.78223701_78223703delinsCTT	GRCh38
NC_000017.10:g.76219782_76219784delinsCTT , CM000679.1:g.76219782_76219784delinsCTT	GRCh37
NC_000017.9:g.73731377_73731379delinsCTT	NCBI36
NG_029069.1:g.14506_14508delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000350051.8:c.*147_*149delinsCTT MANE Select	ENSP00000324180.4:n.*147_*149delinsCTT
ENST00000301633.8:c.*147_*149delinsCTT	ENSP00000301633.3:n.*147_*149delinsCTT
ENST00000350051.7:c.*147_*149delinsCTT	ENSP00000324180.4:n.*147_*149delinsCTT
ENST00000374948.6:c.*44_*46delinsCTT	ENSP00000364086.1:n.*44_*46delinsCTT
ENST00000589892.1:n.592_594delinsCTT
NM_001012270.1:c.*44_*46delinsCTT	NP_001012270.1:n.*44_*46delinsCTT
NM_001012271.1:c.*147_*149delinsCTT	NP_001012271.1:n.*147_*149delinsCTT
NM_001168.2:c.*147_*149delinsCTT	NP_001159.2:n.*147_*149delinsCTT
XR_243654.3:n.778_780delinsCTT
XR_934452.1:n.847_849delinsCTT
XR_243654.5:n.778_780delinsCTT
XR_934452.3:n.847_849delinsCTT
NM_001168.3:c.*147_*149delinsCTT MANE Select	NP_001159.2:n.*147_*149delinsCTT
NM_001012270.2:c.*44_*46delinsCTT	NP_001012270.1:n.*44_*46delinsCTT
NM_001012271.2:c.*147_*149delinsCTT	NP_001012271.1:n.*147_*149delinsCTT