Canonical Allele Identifier: CA401215793

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219716T>G (hg19) ; chr17:g.78223635T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223635T>G , CM000679.2:g.78223635T>G	GRCh38
NC_000017.10:g.76219716T>G , CM000679.1:g.76219716T>G	GRCh37
NC_000017.9:g.73731311T>G	NCBI36
NG_029069.1:g.14440T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*81T>G MANE Select	ENSP00000324180.4:n.*81T>G
ENST00000301633.8:c.*81T>G	ENSP00000301633.3:n.*81T>G
ENST00000350051.7:c.*81T>G	ENSP00000324180.4:n.*81T>G
ENST00000374948.6:c.392T>G	ENSP00000364086.1:p.Val131Gly
ENST00000589892.1:n.526T>G
NM_001012270.1:c.392T>G	NP_001012270.1:p.Val131Gly
NM_001012271.1:c.*81T>G	NP_001012271.1:n.*81T>G
NM_001168.2:c.*81T>G	NP_001159.2:n.*81T>G
XR_243654.3:n.712T>G
XR_934452.1:n.781T>G
XR_243654.5:n.712T>G
XR_934452.3:n.781T>G
NM_001168.3:c.*81T>G MANE Select	NP_001159.2:n.*81T>G
NM_001012270.2:c.392T>G	NP_001012270.1:p.Val131Gly
NM_001012271.2:c.*81T>G	NP_001012271.1:n.*81T>G