Canonical Allele Identifier: CA2276860784

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224116_78224118delinsCAG , CM000679.2:g.78224116_78224118delinsCAG	GRCh38
NC_000017.10:g.76220197_76220199delinsCAG , CM000679.1:g.76220197_76220199delinsCAG	GRCh37
NC_000017.9:g.73731792_73731794delinsCAG	NCBI36
NG_029069.1:g.14921_14923delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*562_*564delinsCAG MANE Select	ENSP00000324180.4:n.*562_*564delinsCAG
ENST00000301633.8:c.*562_*564delinsCAG	ENSP00000301633.3:n.*562_*564delinsCAG
ENST00000350051.7:c.*562_*564delinsCAG	ENSP00000324180.4:n.*562_*564delinsCAG
ENST00000374948.6:c.*459_*461delinsCAG	ENSP00000364086.1:n.*459_*461delinsCAG
NM_001012270.1:c.*459_*461delinsCAG	NP_001012270.1:n.*459_*461delinsCAG
NM_001012271.1:c.*562_*564delinsCAG	NP_001012271.1:n.*562_*564delinsCAG
NM_001168.2:c.*562_*564delinsCAG	NP_001159.2:n.*562_*564delinsCAG
XR_243654.3:n.1193_1195delinsCAG
XR_934452.1:n.1262_1264delinsCAG
XR_243654.5:n.1193_1195delinsCAG
XR_934452.3:n.1262_1264delinsCAG
NM_001168.3:c.*562_*564delinsCAG MANE Select	NP_001159.2:n.*562_*564delinsCAG
NM_001012270.2:c.*459_*461delinsCAG	NP_001012270.1:n.*459_*461delinsCAG
NM_001012271.2:c.*562_*564delinsCAG	NP_001012271.1:n.*562_*564delinsCAG