Canonical Allele Identifier: CA775350842

Gene: BIRC5

Linked Data

• dbSNP Id: rs1378063549
• MyVariant Identifiers: chr17:g.76220136_76220140del (hg19) ; chr17:g.78224055_78224059del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224056_78224060del , CM000679.2:g.78224056_78224060del	GRCh38
NC_000017.10:g.76220137_76220141del , CM000679.1:g.76220137_76220141del	GRCh37
NC_000017.9:g.73731732_73731736del	NCBI36
NG_029069.1:g.14861_14865del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*502_*506del MANE Select	ENSP00000324180.4:n.*502_*506del
ENST00000301633.8:c.*502_*506del	ENSP00000301633.3:n.*502_*506del
ENST00000350051.7:c.*502_*506del	ENSP00000324180.4:n.*502_*506del
ENST00000374948.6:c.*399_*403del	ENSP00000364086.1:n.*399_*403del
NM_001012270.1:c.*399_*403del	NP_001012270.1:n.*399_*403del
NM_001012271.1:c.*502_*506del	NP_001012271.1:n.*502_*506del
NM_001168.2:c.*502_*506del	NP_001159.2:n.*502_*506del
XR_243654.3:n.1133_1137del
XR_934452.1:n.1202_1206del
XR_243654.5:n.1133_1137del
XR_934452.3:n.1202_1206del
NM_001168.3:c.*502_*506del MANE Select	NP_001159.2:n.*502_*506del
NM_001012270.2:c.*399_*403del	NP_001012270.1:n.*399_*403del
NM_001012271.2:c.*502_*506del	NP_001012271.1:n.*502_*506del