Canonical Allele Identifier: CA401215736

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219708C>G (hg19) ; chr17:g.78223627C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223627C>G , CM000679.2:g.78223627C>G	GRCh38
NC_000017.10:g.76219708C>G , CM000679.1:g.76219708C>G	GRCh37
NC_000017.9:g.73731303C>G	NCBI36
NG_029069.1:g.14432C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*73C>G MANE Select	ENSP00000324180.4:n.*73C>G
ENST00000301633.8:c.*73C>G	ENSP00000301633.3:n.*73C>G
ENST00000350051.7:c.*73C>G	ENSP00000324180.4:n.*73C>G
ENST00000374948.6:c.384C>G	ENSP00000364086.1:p.Ser128Arg
ENST00000589892.1:n.518C>G
NM_001012270.1:c.384C>G	NP_001012270.1:p.Ser128Arg
NM_001012271.1:c.*73C>G	NP_001012271.1:n.*73C>G
NM_001168.2:c.*73C>G	NP_001159.2:n.*73C>G
XR_243654.3:n.704C>G
XR_934452.1:n.773C>G
XR_243654.5:n.704C>G
XR_934452.3:n.773C>G
NM_001168.3:c.*73C>G MANE Select	NP_001159.2:n.*73C>G
NM_001012270.2:c.384C>G	NP_001012270.1:p.Ser128Arg
NM_001012271.2:c.*73C>G	NP_001012271.1:n.*73C>G