Canonical Allele Identifier: CA2276860750
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224060_78224064delinsTTTTG , CM000679.2:g.78224060_78224064delinsTTTTG GRCh38
NC_000017.10:g.76220141_76220145delinsTTTTG , CM000679.1:g.76220141_76220145delinsTTTTG GRCh37
NC_000017.9:g.73731736_73731740delinsTTTTG NCBI36
NG_029069.1:g.14865_14869delinsTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*506_*510delinsTTTTG MANE Select ENSP00000324180.4:n.*506_*510delinsTTTTG
ENST00000301633.8:c.*506_*510delinsTTTTG ENSP00000301633.3:n.*506_*510delinsTTTTG
ENST00000350051.7:c.*506_*510delinsTTTTG ENSP00000324180.4:n.*506_*510delinsTTTTG
ENST00000374948.6:c.*403_*407delinsTTTTG ENSP00000364086.1:n.*403_*407delinsTTTTG
NM_001012270.1:c.*403_*407delinsTTTTG NP_001012270.1:n.*403_*407delinsTTTTG
NM_001012271.1:c.*506_*510delinsTTTTG NP_001012271.1:n.*506_*510delinsTTTTG
NM_001168.2:c.*506_*510delinsTTTTG NP_001159.2:n.*506_*510delinsTTTTG
XR_243654.3:n.1137_1141delinsTTTTG
XR_934452.1:n.1206_1210delinsTTTTG
XR_243654.5:n.1137_1141delinsTTTTG
XR_934452.3:n.1206_1210delinsTTTTG
NM_001168.3:c.*506_*510delinsTTTTG MANE Select NP_001159.2:n.*506_*510delinsTTTTG
NM_001012270.2:c.*403_*407delinsTTTTG NP_001012270.1:n.*403_*407delinsTTTTG
NM_001012271.2:c.*506_*510delinsTTTTG NP_001012271.1:n.*506_*510delinsTTTTG