Canonical Allele Identifier: CA401214797

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219592A>G (hg19) ; chr17:g.78223511A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223511A>G , CM000679.2:g.78223511A>G	GRCh38
NC_000017.10:g.76219592A>G , CM000679.1:g.76219592A>G	GRCh37
NC_000017.9:g.73731187A>G	NCBI36
NG_029069.1:g.14316A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.386A>G MANE Select	ENSP00000324180.4:p.Glu129Gly
ENST00000301633.8:c.455A>G	ENSP00000301633.3:p.Glu152Gly
ENST00000350051.7:c.386A>G	ENSP00000324180.4:p.Glu129Gly
ENST00000374948.6:c.268A>G	ENSP00000364086.1:p.Arg90Gly
ENST00000589892.1:n.402A>G
ENST00000590925.6:c.*188A>G	ENSP00000467336.1:n.*188A>G
NM_001012270.1:c.268A>G	NP_001012270.1:p.Arg90Gly
NM_001012271.1:c.455A>G	NP_001012271.1:p.Glu152Gly
NM_001168.2:c.386A>G	NP_001159.2:p.Glu129Gly
XR_243654.3:n.588A>G
XR_934452.1:n.657A>G
XR_243654.5:n.588A>G
XR_934452.3:n.657A>G
NM_001168.3:c.386A>G MANE Select	NP_001159.2:p.Glu129Gly
NM_001012270.2:c.268A>G	NP_001012270.1:p.Arg90Gly
NM_001012271.2:c.455A>G	NP_001012271.1:p.Glu152Gly