Canonical Allele Identifier: CA2276860602
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223762A= , CM000679.2:g.78223762A= GRCh38
NC_000017.10:g.76219843A= , CM000679.1:g.76219843A= GRCh37
NC_000017.9:g.73731438A= NCBI36
NG_029069.1:g.14567A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*208A= MANE Select ENSP00000324180.4:n.*208A=
ENST00000301633.8:c.*208A= ENSP00000301633.3:n.*208A=
ENST00000350051.7:c.*208A= ENSP00000324180.4:n.*208A=
ENST00000374948.6:c.*105A= ENSP00000364086.1:n.*105A=
ENST00000589892.1:n.653A=
NM_001012270.1:c.*105A= NP_001012270.1:n.*105A=
NM_001012271.1:c.*208A= NP_001012271.1:n.*208A=
NM_001168.2:c.*208A= NP_001159.2:n.*208A=
XR_243654.3:n.839A=
XR_934452.1:n.908A=
XR_243654.5:n.839A=
XR_934452.3:n.908A=
NM_001168.3:c.*208A= MANE Select NP_001159.2:n.*208A=
NM_001012270.2:c.*105A= NP_001012270.1:n.*105A=
NM_001012271.2:c.*208A= NP_001012271.1:n.*208A=