Canonical Allele Identifier: CA2276860589
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223716A= , CM000679.2:g.78223716A= GRCh38
NC_000017.10:g.76219797A= , CM000679.1:g.76219797A= GRCh37
NC_000017.9:g.73731392A= NCBI36
NG_029069.1:g.14521A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*162A= MANE Select ENSP00000324180.4:n.*162A=
ENST00000301633.8:c.*162A= ENSP00000301633.3:n.*162A=
ENST00000350051.7:c.*162A= ENSP00000324180.4:n.*162A=
ENST00000374948.6:c.*59A= ENSP00000364086.1:n.*59A=
ENST00000589892.1:n.607A=
NM_001012270.1:c.*59A= NP_001012270.1:n.*59A=
NM_001012271.1:c.*162A= NP_001012271.1:n.*162A=
NM_001168.2:c.*162A= NP_001159.2:n.*162A=
XR_243654.3:n.793A=
XR_934452.1:n.862A=
XR_243654.5:n.793A=
XR_934452.3:n.862A=
NM_001168.3:c.*162A= MANE Select NP_001159.2:n.*162A=
NM_001012270.2:c.*59A= NP_001012270.1:n.*59A=
NM_001012271.2:c.*162A= NP_001012271.1:n.*162A=