Canonical Allele Identifier: CA2276860776
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224102_78224104delinsTGA , CM000679.2:g.78224102_78224104delinsTGA GRCh38
NC_000017.10:g.76220183_76220185delinsTGA , CM000679.1:g.76220183_76220185delinsTGA GRCh37
NC_000017.9:g.73731778_73731780delinsTGA NCBI36
NG_029069.1:g.14907_14909delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*548_*550delinsTGA MANE Select ENSP00000324180.4:n.*548_*550delinsTGA
ENST00000301633.8:c.*548_*550delinsTGA ENSP00000301633.3:n.*548_*550delinsTGA
ENST00000350051.7:c.*548_*550delinsTGA ENSP00000324180.4:n.*548_*550delinsTGA
ENST00000374948.6:c.*445_*447delinsTGA ENSP00000364086.1:n.*445_*447delinsTGA
NM_001012270.1:c.*445_*447delinsTGA NP_001012270.1:n.*445_*447delinsTGA
NM_001012271.1:c.*548_*550delinsTGA NP_001012271.1:n.*548_*550delinsTGA
NM_001168.2:c.*548_*550delinsTGA NP_001159.2:n.*548_*550delinsTGA
XR_243654.3:n.1179_1181delinsTGA
XR_934452.1:n.1248_1250delinsTGA
XR_243654.5:n.1179_1181delinsTGA
XR_934452.3:n.1248_1250delinsTGA
NM_001168.3:c.*548_*550delinsTGA MANE Select NP_001159.2:n.*548_*550delinsTGA
NM_001012270.2:c.*445_*447delinsTGA NP_001012270.1:n.*445_*447delinsTGA
NM_001012271.2:c.*548_*550delinsTGA NP_001012271.1:n.*548_*550delinsTGA