Canonical Allele Identifier: CA8798683
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs761048454

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224009_78224010insAAT , CM000679.2:g.78224009_78224010insAAT GRCh38
NC_000017.10:g.76220090_76220091insAAT , CM000679.1:g.76220090_76220091insAAT GRCh37
NC_000017.9:g.73731685_73731686insAAT NCBI36
NG_029069.1:g.14814_14815insAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*455_*456insAAT MANE Select ENSP00000324180.4:n.*455_*456insAAT
ENST00000301633.8:c.*455_*456insAAT ENSP00000301633.3:n.*455_*456insAAT
ENST00000350051.7:c.*455_*456insAAT ENSP00000324180.4:n.*455_*456insAAT
ENST00000374948.6:c.*352_*353insAAT ENSP00000364086.1:n.*352_*353insAAT
NM_001012270.1:c.*352_*353insAAT NP_001012270.1:n.*352_*353insAAT
NM_001012271.1:c.*455_*456insAAT NP_001012271.1:n.*455_*456insAAT
NM_001168.2:c.*455_*456insAAT NP_001159.2:n.*455_*456insAAT
XR_243654.3:n.1086_1087insAAT
XR_934452.1:n.1155_1156insAAT
XR_243654.5:n.1086_1087insAAT
XR_934452.3:n.1155_1156insAAT
NM_001168.3:c.*455_*456insAAT MANE Select NP_001159.2:n.*455_*456insAAT
NM_001012270.2:c.*352_*353insAAT NP_001012270.1:n.*352_*353insAAT
NM_001012271.2:c.*455_*456insAAT NP_001012271.1:n.*455_*456insAAT