Canonical Allele Identifier: CA2276860755

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224063_78224064delinsTG , CM000679.2:g.78224063_78224064delinsTG	GRCh38
NC_000017.10:g.76220144_76220145delinsTG , CM000679.1:g.76220144_76220145delinsTG	GRCh37
NC_000017.9:g.73731739_73731740delinsTG	NCBI36
NG_029069.1:g.14868_14869delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*509_*510delinsTG MANE Select	ENSP00000324180.4:n.*509_*510delinsTG
ENST00000301633.8:c.*509_*510delinsTG	ENSP00000301633.3:n.*509_*510delinsTG
ENST00000350051.7:c.*509_*510delinsTG	ENSP00000324180.4:n.*509_*510delinsTG
ENST00000374948.6:c.*406_*407delinsTG	ENSP00000364086.1:n.*406_*407delinsTG
NM_001012270.1:c.*406_*407delinsTG	NP_001012270.1:n.*406_*407delinsTG
NM_001012271.1:c.*509_*510delinsTG	NP_001012271.1:n.*509_*510delinsTG
NM_001168.2:c.*509_*510delinsTG	NP_001159.2:n.*509_*510delinsTG
XR_243654.3:n.1140_1141delinsTG
XR_934452.1:n.1209_1210delinsTG
XR_243654.5:n.1140_1141delinsTG
XR_934452.3:n.1209_1210delinsTG
NM_001168.3:c.*509_*510delinsTG MANE Select	NP_001159.2:n.*509_*510delinsTG
NM_001012270.2:c.*406_*407delinsTG	NP_001012270.1:n.*406_*407delinsTG
NM_001012271.2:c.*509_*510delinsTG	NP_001012271.1:n.*509_*510delinsTG