Canonical Allele Identifier: CA775350846

Gene: BIRC5

Linked Data

• dbSNP Id: rs1491093036
• gnomAD v3: 17-78224063-T-TG
• gnomAD v4: 17-78224063-T-TG
• MyVariant Identifiers: chr17:g.76220144_76220145insG (hg19) ; chr17:g.78224063_78224064insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224064dup , CM000679.2:g.78224064dup	GRCh38
NC_000017.10:g.76220145dup , CM000679.1:g.76220145dup	GRCh37
NC_000017.9:g.73731740dup	NCBI36
NG_029069.1:g.14869dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*510dup MANE Select	ENSP00000324180.4:n.*510dup
ENST00000301633.8:c.*510dup	ENSP00000301633.3:n.*510dup
ENST00000350051.7:c.*510dup	ENSP00000324180.4:n.*510dup
ENST00000374948.6:c.*407dup	ENSP00000364086.1:n.*407dup
NM_001012270.1:c.*407dup	NP_001012270.1:n.*407dup
NM_001012271.1:c.*510dup	NP_001012271.1:n.*510dup
NM_001168.2:c.*510dup	NP_001159.2:n.*510dup
XR_243654.3:n.1141dup
XR_934452.1:n.1210dup
XR_243654.5:n.1141dup
XR_934452.3:n.1210dup
NM_001168.3:c.*510dup MANE Select	NP_001159.2:n.*510dup
NM_001012270.2:c.*407dup	NP_001012270.1:n.*407dup
NM_001012271.2:c.*510dup	NP_001012271.1:n.*510dup