Canonical Allele Identifier: CA8798649
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs373086357

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223600C>A , CM000679.2:g.78223600C>A GRCh38
NC_000017.10:g.76219681C>A , CM000679.1:g.76219681C>A GRCh37
NC_000017.9:g.73731276C>A NCBI36
NG_029069.1:g.14405C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*46C>A MANE Select ENSP00000324180.4:n.*46C>A
ENST00000301633.8:c.*46C>A ENSP00000301633.3:n.*46C>A
ENST00000350051.7:c.*46C>A ENSP00000324180.4:n.*46C>A
ENST00000374948.6:c.357C>A ENSP00000364086.1:p.Phe119Leu
ENST00000589892.1:n.491C>A
NM_001012270.1:c.357C>A NP_001012270.1:p.Phe119Leu
NM_001012271.1:c.*46C>A NP_001012271.1:n.*46C>A
NM_001168.2:c.*46C>A NP_001159.2:n.*46C>A
XR_243654.3:n.677C>A
XR_934452.1:n.746C>A
XR_243654.5:n.677C>A
XR_934452.3:n.746C>A
NM_001168.3:c.*46C>A MANE Select NP_001159.2:n.*46C>A
NM_001012270.2:c.357C>A NP_001012270.1:p.Phe119Leu
NM_001012271.2:c.*46C>A NP_001012271.1:n.*46C>A