Canonical Allele Identifier: CA986568359

Gene: BIRC5

Linked Data

• dbSNP Id: rs1567867388
• gnomAD v3: 17-78224051-G-GTGTTTTTTTTTTTTT
• gnomAD v4: 17-78224051-G-GTGTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224052_78224053insGTTTTTTTTTTTTTT , CM000679.2:g.78224052_78224053insGTTTTTTTTTTTTTT	GRCh38
NC_000017.10:g.76220133_76220134insGTTTTTTTTTTTTTT , CM000679.1:g.76220133_76220134insGTTTTTTTTTTTTTT	GRCh37
NC_000017.9:g.73731728_73731729insGTTTTTTTTTTTTTT	NCBI36
NG_029069.1:g.14857_14858insGTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*498_*499insGTTTTTTTTTTTTTT MANE Select	ENSP00000324180.4:n.*498_*499insGTTTTTTTTTTTTTT
ENST00000301633.8:c.*498_*499insGTTTTTTTTTTTTTT	ENSP00000301633.3:n.*498_*499insGTTTTTTTTTTTTTT
ENST00000350051.7:c.*498_*499insGTTTTTTTTTTTTTT	ENSP00000324180.4:n.*498_*499insGTTTTTTTTTTTTTT
ENST00000374948.6:c.*395_*396insGTTTTTTTTTTTTTT	ENSP00000364086.1:n.*395_*396insGTTTTTTTTTTTTTT
NM_001012270.1:c.*395_*396insGTTTTTTTTTTTTTT	NP_001012270.1:n.*395_*396insGTTTTTTTTTTTTTT
NM_001012271.1:c.*498_*499insGTTTTTTTTTTTTTT	NP_001012271.1:n.*498_*499insGTTTTTTTTTTTTTT
NM_001168.2:c.*498_*499insGTTTTTTTTTTTTTT	NP_001159.2:n.*498_*499insGTTTTTTTTTTTTTT
XR_243654.3:n.1129_1130insGTTTTTTTTTTTTTT
XR_934452.1:n.1198_1199insGTTTTTTTTTTTTTT
XR_243654.5:n.1129_1130insGTTTTTTTTTTTTTT
XR_934452.3:n.1198_1199insGTTTTTTTTTTTTTT
NM_001168.3:c.*498_*499insGTTTTTTTTTTTTTT MANE Select	NP_001159.2:n.*498_*499insGTTTTTTTTTTTTTT
NM_001012270.2:c.*395_*396insGTTTTTTTTTTTTTT	NP_001012270.1:n.*395_*396insGTTTTTTTTTTTTTT
NM_001012271.2:c.*498_*499insGTTTTTTTTTTTTTT	NP_001012271.1:n.*498_*499insGTTTTTTTTTTTTTT