Canonical Allele Identifier: CA656884494

Gene: BIRC5

Linked Data

• COSMIC: COSN15657350

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224065_78224066insG , CM000679.2:g.78224065_78224066insG	GRCh38
NC_000017.10:g.76220146_76220147insG , CM000679.1:g.76220146_76220147insG	GRCh37
NC_000017.9:g.73731741_73731742insG	NCBI36
NG_029069.1:g.14870_14871insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*511_*512insG MANE Select	ENSP00000324180.4:n.*511_*512insG
ENST00000301633.8:c.*511_*512insG	ENSP00000301633.3:n.*511_*512insG
ENST00000350051.7:c.*511_*512insG	ENSP00000324180.4:n.*511_*512insG
ENST00000374948.6:c.*408_*409insG	ENSP00000364086.1:n.*408_*409insG
NM_001012270.1:c.*408_*409insG	NP_001012270.1:n.*408_*409insG
NM_001012271.1:c.*511_*512insG	NP_001012271.1:n.*511_*512insG
NM_001168.2:c.*511_*512insG	NP_001159.2:n.*511_*512insG
XR_243654.3:n.1142_1143insG
XR_934452.1:n.1211_1212insG
XR_243654.5:n.1142_1143insG
XR_934452.3:n.1211_1212insG
NM_001168.3:c.*511_*512insG MANE Select	NP_001159.2:n.*511_*512insG
NM_001012270.2:c.*408_*409insG	NP_001012270.1:n.*408_*409insG
NM_001012271.2:c.*511_*512insG	NP_001012271.1:n.*511_*512insG