Canonical Allele Identifier: CA2276860738

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224054_78224055delinsGT , CM000679.2:g.78224054_78224055delinsGT	GRCh38
NC_000017.10:g.76220135_76220136delinsGT , CM000679.1:g.76220135_76220136delinsGT	GRCh37
NC_000017.9:g.73731730_73731731delinsGT	NCBI36
NG_029069.1:g.14859_14860delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*500_*501delinsGT MANE Select	ENSP00000324180.4:n.*500_*501delinsGT
ENST00000301633.8:c.*500_*501delinsGT	ENSP00000301633.3:n.*500_*501delinsGT
ENST00000350051.7:c.*500_*501delinsGT	ENSP00000324180.4:n.*500_*501delinsGT
ENST00000374948.6:c.*397_*398delinsGT	ENSP00000364086.1:n.*397_*398delinsGT
NM_001012270.1:c.*397_*398delinsGT	NP_001012270.1:n.*397_*398delinsGT
NM_001012271.1:c.*500_*501delinsGT	NP_001012271.1:n.*500_*501delinsGT
NM_001168.2:c.*500_*501delinsGT	NP_001159.2:n.*500_*501delinsGT
XR_243654.3:n.1131_1132delinsGT
XR_934452.1:n.1200_1201delinsGT
XR_243654.5:n.1131_1132delinsGT
XR_934452.3:n.1200_1201delinsGT
NM_001168.3:c.*500_*501delinsGT MANE Select	NP_001159.2:n.*500_*501delinsGT
NM_001012270.2:c.*397_*398delinsGT	NP_001012270.1:n.*397_*398delinsGT
NM_001012271.2:c.*500_*501delinsGT	NP_001012271.1:n.*500_*501delinsGT