Canonical Allele Identifier: CA2276860753
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224062_78224064delinsTTG , CM000679.2:g.78224062_78224064delinsTTG GRCh38
NC_000017.10:g.76220143_76220145delinsTTG , CM000679.1:g.76220143_76220145delinsTTG GRCh37
NC_000017.9:g.73731738_73731740delinsTTG NCBI36
NG_029069.1:g.14867_14869delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*508_*510delinsTTG MANE Select ENSP00000324180.4:n.*508_*510delinsTTG
ENST00000301633.8:c.*508_*510delinsTTG ENSP00000301633.3:n.*508_*510delinsTTG
ENST00000350051.7:c.*508_*510delinsTTG ENSP00000324180.4:n.*508_*510delinsTTG
ENST00000374948.6:c.*405_*407delinsTTG ENSP00000364086.1:n.*405_*407delinsTTG
NM_001012270.1:c.*405_*407delinsTTG NP_001012270.1:n.*405_*407delinsTTG
NM_001012271.1:c.*508_*510delinsTTG NP_001012271.1:n.*508_*510delinsTTG
NM_001168.2:c.*508_*510delinsTTG NP_001159.2:n.*508_*510delinsTTG
XR_243654.3:n.1139_1141delinsTTG
XR_934452.1:n.1208_1210delinsTTG
XR_243654.5:n.1139_1141delinsTTG
XR_934452.3:n.1208_1210delinsTTG
NM_001168.3:c.*508_*510delinsTTG MANE Select NP_001159.2:n.*508_*510delinsTTG
NM_001012270.2:c.*405_*407delinsTTG NP_001012270.1:n.*405_*407delinsTTG
NM_001012271.2:c.*508_*510delinsTTG NP_001012271.1:n.*508_*510delinsTTG