Canonical Allele Identifier: CA502087147

Gene: BIRC5

Linked Data

• dbSNP Id: rs1197876785
• MyVariant Identifiers: chr17:g.76220131_76220135del (hg19) ; chr17:g.78224050_78224054del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224054_78224058del , CM000679.2:g.78224054_78224058del	GRCh38
NC_000017.10:g.76220135_76220139del , CM000679.1:g.76220135_76220139del	GRCh37
NC_000017.9:g.73731730_73731734del	NCBI36
NG_029069.1:g.14859_14863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*500_*504del MANE Select	ENSP00000324180.4:n.*500_*504del
ENST00000301633.8:c.*500_*504del	ENSP00000301633.3:n.*500_*504del
ENST00000350051.7:c.*500_*504del	ENSP00000324180.4:n.*500_*504del
ENST00000374948.6:c.*397_*401del	ENSP00000364086.1:n.*397_*401del
NM_001012270.1:c.*397_*401del	NP_001012270.1:n.*397_*401del
NM_001012271.1:c.*500_*504del	NP_001012271.1:n.*500_*504del
NM_001168.2:c.*500_*504del	NP_001159.2:n.*500_*504del
XR_243654.3:n.1131_1135del
XR_934452.1:n.1200_1204del
XR_243654.5:n.1131_1135del
XR_934452.3:n.1200_1204del
NM_001168.3:c.*500_*504del MANE Select	NP_001159.2:n.*500_*504del
NM_001012270.2:c.*397_*401del	NP_001012270.1:n.*397_*401del
NM_001012271.2:c.*500_*504del	NP_001012271.1:n.*500_*504del