Canonical Allele Identifier: CA401215322

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219656T>A (hg19) ; chr17:g.78223575T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223575T>A , CM000679.2:g.78223575T>A	GRCh38
NC_000017.10:g.76219656T>A , CM000679.1:g.76219656T>A	GRCh37
NC_000017.9:g.73731251T>A	NCBI36
NG_029069.1:g.14380T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*21T>A MANE Select	ENSP00000324180.4:n.*21T>A
ENST00000301633.8:c.*21T>A	ENSP00000301633.3:n.*21T>A
ENST00000350051.7:c.*21T>A	ENSP00000324180.4:n.*21T>A
ENST00000374948.6:c.332T>A	ENSP00000364086.1:p.Leu111Gln
ENST00000589892.1:n.466T>A
NM_001012270.1:c.332T>A	NP_001012270.1:p.Leu111Gln
NM_001012271.1:c.*21T>A	NP_001012271.1:n.*21T>A
NM_001168.2:c.*21T>A	NP_001159.2:n.*21T>A
XR_243654.3:n.652T>A
XR_934452.1:n.721T>A
XR_243654.5:n.652T>A
XR_934452.3:n.721T>A
NM_001168.3:c.*21T>A MANE Select	NP_001159.2:n.*21T>A
NM_001012270.2:c.332T>A	NP_001012270.1:p.Leu111Gln
NM_001012271.2:c.*21T>A	NP_001012271.1:n.*21T>A