Canonical Allele Identifier: CA294307589

Gene: BIRC5

Linked Data

• dbSNP Id: rs902394767
• MyVariant Identifiers: chr17:g.76220179G>A (hg19) ; chr17:g.78224098G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224098G>A , CM000679.2:g.78224098G>A	GRCh38
NC_000017.10:g.76220179G>A , CM000679.1:g.76220179G>A	GRCh37
NC_000017.9:g.73731774G>A	NCBI36
NG_029069.1:g.14903G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*544G>A MANE Select	ENSP00000324180.4:n.*544G>A
ENST00000301633.8:c.*544G>A	ENSP00000301633.3:n.*544G>A
ENST00000350051.7:c.*544G>A	ENSP00000324180.4:n.*544G>A
ENST00000374948.6:c.*441G>A	ENSP00000364086.1:n.*441G>A
NM_001012270.1:c.*441G>A	NP_001012270.1:n.*441G>A
NM_001012271.1:c.*544G>A	NP_001012271.1:n.*544G>A
NM_001168.2:c.*544G>A	NP_001159.2:n.*544G>A
XR_243654.3:n.1175G>A
XR_934452.1:n.1244G>A
XR_243654.5:n.1175G>A
XR_934452.3:n.1244G>A
NM_001168.3:c.*544G>A MANE Select	NP_001159.2:n.*544G>A
NM_001012270.2:c.*441G>A	NP_001012270.1:n.*441G>A
NM_001012271.2:c.*544G>A	NP_001012271.1:n.*544G>A