Canonical Allele Identifier: CA2276860769

Gene: BIRC5

Linked Data

• dbSNP Id: rs2076534291
• gnomAD v4: 17-78224084-T-TGCATGACTTGTGTGTGATGAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224086_78224107dup , CM000679.2:g.78224086_78224107dup	GRCh38
NC_000017.10:g.76220167_76220188dup , CM000679.1:g.76220167_76220188dup	GRCh37
NC_000017.9:g.73731762_73731783dup	NCBI36
NG_029069.1:g.14891_14912dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*532_*553dup MANE Select	ENSP00000324180.4:n.*532_*553dup
ENST00000301633.8:c.*532_*553dup	ENSP00000301633.3:n.*532_*553dup
ENST00000350051.7:c.*532_*553dup	ENSP00000324180.4:n.*532_*553dup
ENST00000374948.6:c.*429_*450dup	ENSP00000364086.1:n.*429_*450dup
NM_001012270.1:c.*429_*450dup	NP_001012270.1:n.*429_*450dup
NM_001012271.1:c.*532_*553dup	NP_001012271.1:n.*532_*553dup
NM_001168.2:c.*532_*553dup	NP_001159.2:n.*532_*553dup
XR_243654.3:n.1163_1184dup
XR_934452.1:n.1232_1253dup
XR_243654.5:n.1163_1184dup
XR_934452.3:n.1232_1253dup
NM_001168.3:c.*532_*553dup MANE Select	NP_001159.2:n.*532_*553dup
NM_001012270.2:c.*429_*450dup	NP_001012270.1:n.*429_*450dup
NM_001012271.2:c.*532_*553dup	NP_001012271.1:n.*532_*553dup