Canonical Allele Identifier: CA2640134538

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78223983-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223983T>C , CM000679.2:g.78223983T>C	GRCh38
NC_000017.10:g.76220064T>C , CM000679.1:g.76220064T>C	GRCh37
NC_000017.9:g.73731659T>C	NCBI36
NG_029069.1:g.14788T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*429T>C MANE Select	ENSP00000324180.4:n.*429T>C
ENST00000301633.8:c.*429T>C	ENSP00000301633.3:n.*429T>C
ENST00000350051.7:c.*429T>C	ENSP00000324180.4:n.*429T>C
ENST00000374948.6:c.*326T>C	ENSP00000364086.1:n.*326T>C
NM_001012270.1:c.*326T>C	NP_001012270.1:n.*326T>C
NM_001012271.1:c.*429T>C	NP_001012271.1:n.*429T>C
NM_001168.2:c.*429T>C	NP_001159.2:n.*429T>C
XR_243654.3:n.1060T>C
XR_934452.1:n.1129T>C
XR_243654.5:n.1060T>C
XR_934452.3:n.1129T>C
NM_001168.3:c.*429T>C MANE Select	NP_001159.2:n.*429T>C
NM_001012270.2:c.*326T>C	NP_001012270.1:n.*326T>C
NM_001012271.2:c.*429T>C	NP_001012271.1:n.*429T>C