Canonical Allele Identifier: CA2276860485
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223437G= , CM000679.2:g.78223437G= GRCh38
NC_000017.10:g.76219518G= , CM000679.1:g.76219518G= GRCh37
NC_000017.9:g.73731113G= NCBI36
NG_029069.1:g.14242G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.340-28G= MANE Select ENSP00000324180.4:n.340-28G=
ENST00000301633.8:c.409-28G= ENSP00000301633.3:n.409-28G=
ENST00000350051.7:c.340-28G= ENSP00000324180.4:n.340-28G=
ENST00000374948.6:c.222-28G= ENSP00000364086.1:n.222-28G=
ENST00000589892.1:n.356-28G=
ENST00000590925.6:c.*142-28G= ENSP00000467336.1:n.*142-28G=
NM_001012270.1:c.222-28G= NP_001012270.1:n.222-28G=
NM_001012271.1:c.409-28G= NP_001012271.1:n.409-28G=
NM_001168.2:c.340-28G= NP_001159.2:n.340-28G=
XR_243654.3:n.542-28G=
XR_934452.1:n.611-28G=
XR_243654.5:n.542-28G=
XR_934452.3:n.611-28G=
NM_001168.3:c.340-28G= MANE Select NP_001159.2:n.340-28G=
NM_001012270.2:c.222-28G= NP_001012270.1:n.222-28G=
NM_001012271.2:c.409-28G= NP_001012271.1:n.409-28G=