Canonical Allele Identifier: CA401214927

Gene: BIRC5

Linked Data

• dbSNP Id: rs1599033723
• MyVariant Identifiers: chr17:g.76219606G>C (hg19) ; chr17:g.78223525G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.400G>C MANE Select	ENSP00000324180.4:p.Ala134Pro
ENST00000301633.8:c.469G>C	ENSP00000301633.3:p.Ala157Pro
ENST00000350051.7:c.400G>C	ENSP00000324180.4:p.Ala134Pro
ENST00000374948.6:c.282G>C	ENSP00000364086.1:p.Val94=
ENST00000589892.1:n.416G>C
ENST00000590925.6:c.*202G>C	ENSP00000467336.1:n.*202G>C
NM_001012270.1:c.282G>C	NP_001012270.1:p.Val94=
NM_001012271.1:c.469G>C	NP_001012271.1:p.Ala157Pro
NM_001168.2:c.400G>C	NP_001159.2:p.Ala134Pro
XR_243654.3:n.602G>C
XR_934452.1:n.671G>C
XR_243654.5:n.602G>C
XR_934452.3:n.671G>C
NM_001168.3:c.400G>C MANE Select	NP_001159.2:p.Ala134Pro
NM_001012270.2:c.282G>C	NP_001012270.1:p.Val94=
NM_001012271.2:c.469G>C	NP_001012271.1:p.Ala157Pro