Canonical Allele Identifier: CA2640134139

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78223791-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223791_78223792insC , CM000679.2:g.78223791_78223792insC	GRCh38
NC_000017.10:g.76219872_76219873insC , CM000679.1:g.76219872_76219873insC	GRCh37
NC_000017.9:g.73731467_73731468insC	NCBI36
NG_029069.1:g.14596_14597insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*237_*238insC MANE Select	ENSP00000324180.4:n.*237_*238insC
ENST00000301633.8:c.*237_*238insC	ENSP00000301633.3:n.*237_*238insC
ENST00000350051.7:c.*237_*238insC	ENSP00000324180.4:n.*237_*238insC
ENST00000374948.6:c.*134_*135insC	ENSP00000364086.1:n.*134_*135insC
ENST00000589892.1:n.682_683insC
NM_001012270.1:c.*134_*135insC	NP_001012270.1:n.*134_*135insC
NM_001012271.1:c.*237_*238insC	NP_001012271.1:n.*237_*238insC
NM_001168.2:c.*237_*238insC	NP_001159.2:n.*237_*238insC
XR_243654.3:n.868_869insC
XR_934452.1:n.937_938insC
XR_243654.5:n.868_869insC
XR_934452.3:n.937_938insC
NM_001168.3:c.*237_*238insC MANE Select	NP_001159.2:n.*237_*238insC
NM_001012270.2:c.*134_*135insC	NP_001012270.1:n.*134_*135insC
NM_001012271.2:c.*237_*238insC	NP_001012271.1:n.*237_*238insC