Canonical Allele Identifier: CA401214924

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219606G>A (hg19) ; chr17:g.78223525G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223525G>A , CM000679.2:g.78223525G>A	GRCh38
NC_000017.10:g.76219606G>A , CM000679.1:g.76219606G>A	GRCh37
NC_000017.9:g.73731201G>A	NCBI36
NG_029069.1:g.14330G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.400G>A MANE Select	ENSP00000324180.4:p.Ala134Thr
ENST00000301633.8:c.469G>A	ENSP00000301633.3:p.Ala157Thr
ENST00000350051.7:c.400G>A	ENSP00000324180.4:p.Ala134Thr
ENST00000374948.6:c.282G>A	ENSP00000364086.1:p.Val94=
ENST00000589892.1:n.416G>A
ENST00000590925.6:c.*202G>A	ENSP00000467336.1:n.*202G>A
NM_001012270.1:c.282G>A	NP_001012270.1:p.Val94=
NM_001012271.1:c.469G>A	NP_001012271.1:p.Ala157Thr
NM_001168.2:c.400G>A	NP_001159.2:p.Ala134Thr
XR_243654.3:n.602G>A
XR_934452.1:n.671G>A
XR_243654.5:n.602G>A
XR_934452.3:n.671G>A
NM_001168.3:c.400G>A MANE Select	NP_001159.2:p.Ala134Thr
NM_001012270.2:c.282G>A	NP_001012270.1:p.Val94=
NM_001012271.2:c.469G>A	NP_001012271.1:p.Ala157Thr