Canonical Allele Identifier: CA775350564
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs1317762842

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223389T>A , CM000679.2:g.78223389T>A GRCh38
NC_000017.10:g.76219470T>A , CM000679.1:g.76219470T>A GRCh37
NC_000017.9:g.73731065T>A NCBI36
NG_029069.1:g.14194T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.340-76T>A MANE Select ENSP00000324180.4:n.340-76T>A
ENST00000301633.8:c.409-76T>A ENSP00000301633.3:n.409-76T>A
ENST00000350051.7:c.340-76T>A ENSP00000324180.4:n.340-76T>A
ENST00000374948.6:c.222-76T>A ENSP00000364086.1:n.222-76T>A
ENST00000589892.1:n.356-76T>A
ENST00000590925.6:c.*142-76T>A ENSP00000467336.1:n.*142-76T>A
NM_001012270.1:c.222-76T>A NP_001012270.1:n.222-76T>A
NM_001012271.1:c.409-76T>A NP_001012271.1:n.409-76T>A
NM_001168.2:c.340-76T>A NP_001159.2:n.340-76T>A
XR_243654.3:n.542-76T>A
XR_934452.1:n.611-76T>A
XR_243654.5:n.542-76T>A
XR_934452.3:n.611-76T>A
NM_001168.3:c.340-76T>A MANE Select NP_001159.2:n.340-76T>A
NM_001012270.2:c.222-76T>A NP_001012270.1:n.222-76T>A
NM_001012271.2:c.409-76T>A NP_001012271.1:n.409-76T>A