Canonical Allele Identifier: CA2640134781

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78224060-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224060_78224061insG , CM000679.2:g.78224060_78224061insG	GRCh38
NC_000017.10:g.76220141_76220142insG , CM000679.1:g.76220141_76220142insG	GRCh37
NC_000017.9:g.73731736_73731737insG	NCBI36
NG_029069.1:g.14865_14866insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*506_*507insG MANE Select	ENSP00000324180.4:n.*506_*507insG
ENST00000301633.8:c.*506_*507insG	ENSP00000301633.3:n.*506_*507insG
ENST00000350051.7:c.*506_*507insG	ENSP00000324180.4:n.*506_*507insG
ENST00000374948.6:c.*403_*404insG	ENSP00000364086.1:n.*403_*404insG
NM_001012270.1:c.*403_*404insG	NP_001012270.1:n.*403_*404insG
NM_001012271.1:c.*506_*507insG	NP_001012271.1:n.*506_*507insG
NM_001168.2:c.*506_*507insG	NP_001159.2:n.*506_*507insG
XR_243654.3:n.1137_1138insG
XR_934452.1:n.1206_1207insG
XR_243654.5:n.1137_1138insG
XR_934452.3:n.1206_1207insG
NM_001168.3:c.*506_*507insG MANE Select	NP_001159.2:n.*506_*507insG
NM_001012270.2:c.*403_*404insG	NP_001012270.1:n.*403_*404insG
NM_001012271.2:c.*506_*507insG	NP_001012271.1:n.*506_*507insG