Canonical Allele Identifier: CA2276860745
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224056_78224060delinsGTTTT , CM000679.2:g.78224056_78224060delinsGTTTT GRCh38
NC_000017.10:g.76220137_76220141delinsGTTTT , CM000679.1:g.76220137_76220141delinsGTTTT GRCh37
NC_000017.9:g.73731732_73731736delinsGTTTT NCBI36
NG_029069.1:g.14861_14865delinsGTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*502_*506delinsGTTTT MANE Select ENSP00000324180.4:n.*502_*506delinsGTTTT
ENST00000301633.8:c.*502_*506delinsGTTTT ENSP00000301633.3:n.*502_*506delinsGTTTT
ENST00000350051.7:c.*502_*506delinsGTTTT ENSP00000324180.4:n.*502_*506delinsGTTTT
ENST00000374948.6:c.*399_*403delinsGTTTT ENSP00000364086.1:n.*399_*403delinsGTTTT
NM_001012270.1:c.*399_*403delinsGTTTT NP_001012270.1:n.*399_*403delinsGTTTT
NM_001012271.1:c.*502_*506delinsGTTTT NP_001012271.1:n.*502_*506delinsGTTTT
NM_001168.2:c.*502_*506delinsGTTTT NP_001159.2:n.*502_*506delinsGTTTT
XR_243654.3:n.1133_1137delinsGTTTT
XR_934452.1:n.1202_1206delinsGTTTT
XR_243654.5:n.1133_1137delinsGTTTT
XR_934452.3:n.1202_1206delinsGTTTT
NM_001168.3:c.*502_*506delinsGTTTT MANE Select NP_001159.2:n.*502_*506delinsGTTTT
NM_001012270.2:c.*399_*403delinsGTTTT NP_001012270.1:n.*399_*403delinsGTTTT
NM_001012271.2:c.*502_*506delinsGTTTT NP_001012271.1:n.*502_*506delinsGTTTT