Canonical Allele Identifier: CA986568589

Gene: BIRC5

Linked Data

• dbSNP Id: rs2076534693
• gnomAD v3: 17-78224141-T-C
• gnomAD v4: 17-78224141-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224141T>C , CM000679.2:g.78224141T>C	GRCh38
NC_000017.10:g.76220222T>C , CM000679.1:g.76220222T>C	GRCh37
NC_000017.9:g.73731817T>C	NCBI36
NG_029069.1:g.14946T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*587T>C MANE Select	ENSP00000324180.4:n.*587T>C
ENST00000301633.8:c.*587T>C	ENSP00000301633.3:n.*587T>C
ENST00000350051.7:c.*587T>C	ENSP00000324180.4:n.*587T>C
ENST00000374948.6:c.*484T>C	ENSP00000364086.1:n.*484T>C
NM_001012270.1:c.*484T>C	NP_001012270.1:n.*484T>C
NM_001012271.1:c.*587T>C	NP_001012271.1:n.*587T>C
NM_001168.2:c.*587T>C	NP_001159.2:n.*587T>C
XR_243654.3:n.1218T>C
XR_934452.1:n.1287T>C
XR_243654.5:n.1218T>C
XR_934452.3:n.1287T>C
NM_001168.3:c.*587T>C MANE Select	NP_001159.2:n.*587T>C
NM_001012270.2:c.*484T>C	NP_001012270.1:n.*484T>C
NM_001012271.2:c.*587T>C	NP_001012271.1:n.*587T>C