Canonical Allele Identifier: CA2741557686
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224052_78224053insGTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000679.2:g.78224052_78224053insGTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000017.10:g.76220133_76220134insGTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000679.1:g.76220133_76220134insGTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000017.9:g.73731728_73731729insGTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_029069.1:g.14857_14858insGTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000324180.4:n.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000301633.8:c.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000301633.3:n.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000350051.7:c.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000324180.4:n.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000374948.6:c.*395_*396insGTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000364086.1:n.*395_*396insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001012270.1:c.*395_*396insGTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001012270.1:n.*395_*396insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001012271.1:c.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001012271.1:n.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001168.2:c.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001159.2:n.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_243654.3:n.1129_1130insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_934452.1:n.1198_1199insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_243654.5:n.1129_1130insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_934452.3:n.1198_1199insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001168.3:c.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_001159.2:n.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001012270.2:c.*395_*396insGTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001012270.1:n.*395_*396insGTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001012271.2:c.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001012271.1:n.*498_*499insGTTTTTTTTTTTTTTTTTTTTTTTTTTT