Canonical Allele Identifier: CA2640133824

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78223733-C-CCACT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223733_78223734insCACT , CM000679.2:g.78223733_78223734insCACT	GRCh38
NC_000017.10:g.76219814_76219815insCACT , CM000679.1:g.76219814_76219815insCACT	GRCh37
NC_000017.9:g.73731409_73731410insCACT	NCBI36
NG_029069.1:g.14538_14539insCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*179_*180insCACT MANE Select	ENSP00000324180.4:n.*179_*180insCACT
ENST00000301633.8:c.*179_*180insCACT	ENSP00000301633.3:n.*179_*180insCACT
ENST00000350051.7:c.*179_*180insCACT	ENSP00000324180.4:n.*179_*180insCACT
ENST00000374948.6:c.*76_*77insCACT	ENSP00000364086.1:n.*76_*77insCACT
ENST00000589892.1:n.624_625insCACT
NM_001012270.1:c.*76_*77insCACT	NP_001012270.1:n.*76_*77insCACT
NM_001012271.1:c.*179_*180insCACT	NP_001012271.1:n.*179_*180insCACT
NM_001168.2:c.*179_*180insCACT	NP_001159.2:n.*179_*180insCACT
XR_243654.3:n.810_811insCACT
XR_934452.1:n.879_880insCACT
XR_243654.5:n.810_811insCACT
XR_934452.3:n.879_880insCACT
NM_001168.3:c.*179_*180insCACT MANE Select	NP_001159.2:n.*179_*180insCACT
NM_001012270.2:c.*76_*77insCACT	NP_001012270.1:n.*76_*77insCACT
NM_001012271.2:c.*179_*180insCACT	NP_001012271.1:n.*179_*180insCACT