Canonical Allele Identifier: CA2276860622
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223810T= , CM000679.2:g.78223810T= GRCh38
NC_000017.10:g.76219891T= , CM000679.1:g.76219891T= GRCh37
NC_000017.9:g.73731486T= NCBI36
NG_029069.1:g.14615T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*256T= MANE Select ENSP00000324180.4:n.*256T=
ENST00000301633.8:c.*256T= ENSP00000301633.3:n.*256T=
ENST00000350051.7:c.*256T= ENSP00000324180.4:n.*256T=
ENST00000374948.6:c.*153T= ENSP00000364086.1:n.*153T=
ENST00000589892.1:n.701T=
NM_001012270.1:c.*153T= NP_001012270.1:n.*153T=
NM_001012271.1:c.*256T= NP_001012271.1:n.*256T=
NM_001168.2:c.*256T= NP_001159.2:n.*256T=
XR_243654.3:n.887T=
XR_934452.1:n.956T=
XR_243654.5:n.887T=
XR_934452.3:n.956T=
NM_001168.3:c.*256T= MANE Select NP_001159.2:n.*256T=
NM_001012270.2:c.*153T= NP_001012270.1:n.*153T=
NM_001012271.2:c.*256T= NP_001012271.1:n.*256T=