Canonical Allele Identifier: CA2276860690
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224018_78224019delinsAC , CM000679.2:g.78224018_78224019delinsAC GRCh38
NC_000017.10:g.76220099_76220100delinsAC , CM000679.1:g.76220099_76220100delinsAC GRCh37
NC_000017.9:g.73731694_73731695delinsAC NCBI36
NG_029069.1:g.14823_14824delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*464_*465delinsAC MANE Select ENSP00000324180.4:n.*464_*465delinsAC
ENST00000301633.8:c.*464_*465delinsAC ENSP00000301633.3:n.*464_*465delinsAC
ENST00000350051.7:c.*464_*465delinsAC ENSP00000324180.4:n.*464_*465delinsAC
ENST00000374948.6:c.*361_*362delinsAC ENSP00000364086.1:n.*361_*362delinsAC
NM_001012270.1:c.*361_*362delinsAC NP_001012270.1:n.*361_*362delinsAC
NM_001012271.1:c.*464_*465delinsAC NP_001012271.1:n.*464_*465delinsAC
NM_001168.2:c.*464_*465delinsAC NP_001159.2:n.*464_*465delinsAC
XR_243654.3:n.1095_1096delinsAC
XR_934452.1:n.1164_1165delinsAC
XR_243654.5:n.1095_1096delinsAC
XR_934452.3:n.1164_1165delinsAC
NM_001168.3:c.*464_*465delinsAC MANE Select NP_001159.2:n.*464_*465delinsAC
NM_001012270.2:c.*361_*362delinsAC NP_001012270.1:n.*361_*362delinsAC
NM_001012271.2:c.*464_*465delinsAC NP_001012271.1:n.*464_*465delinsAC