Canonical Allele Identifier: CA2581326652
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223442A>C , CM000679.2:g.78223442A>C GRCh38
NC_000017.10:g.76219523A>C , CM000679.1:g.76219523A>C GRCh37
NC_000017.9:g.73731118A>C NCBI36
NG_029069.1:g.14247A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.340-23A>C MANE Select ENSP00000324180.4:n.340-23A>C
ENST00000301633.8:c.409-23A>C ENSP00000301633.3:n.409-23A>C
ENST00000350051.7:c.340-23A>C ENSP00000324180.4:n.340-23A>C
ENST00000374948.6:c.222-23A>C ENSP00000364086.1:n.222-23A>C
ENST00000589892.1:n.356-23A>C
ENST00000590925.6:c.*142-23A>C ENSP00000467336.1:n.*142-23A>C
NM_001012270.1:c.222-23A>C NP_001012270.1:n.222-23A>C
NM_001012271.1:c.409-23A>C NP_001012271.1:n.409-23A>C
NM_001168.2:c.340-23A>C NP_001159.2:n.340-23A>C
XR_243654.3:n.542-23A>C
XR_934452.1:n.611-23A>C
XR_243654.5:n.542-23A>C
XR_934452.3:n.611-23A>C
NM_001168.3:c.340-23A>C MANE Select NP_001159.2:n.340-23A>C
NM_001012270.2:c.222-23A>C NP_001012270.1:n.222-23A>C
NM_001012271.2:c.409-23A>C NP_001012271.1:n.409-23A>C