Canonical Allele Identifier: CA2276860785

Gene: BIRC5

Linked Data

• dbSNP Id: rs2076534521

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224119_78224120del , CM000679.2:g.78224119_78224120del	GRCh38
NC_000017.10:g.76220200_76220201del , CM000679.1:g.76220200_76220201del	GRCh37
NC_000017.9:g.73731795_73731796del	NCBI36
NG_029069.1:g.14924_14925del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*565_*566del MANE Select	ENSP00000324180.4:n.*565_*566del
ENST00000301633.8:c.*565_*566del	ENSP00000301633.3:n.*565_*566del
ENST00000350051.7:c.*565_*566del	ENSP00000324180.4:n.*565_*566del
ENST00000374948.6:c.*462_*463del	ENSP00000364086.1:n.*462_*463del
NM_001012270.1:c.*462_*463del	NP_001012270.1:n.*462_*463del
NM_001012271.1:c.*565_*566del	NP_001012271.1:n.*565_*566del
NM_001168.2:c.*565_*566del	NP_001159.2:n.*565_*566del
XR_243654.3:n.1196_1197del
XR_934452.1:n.1265_1266del
XR_243654.5:n.1196_1197del
XR_934452.3:n.1265_1266del
NM_001168.3:c.*565_*566del MANE Select	NP_001159.2:n.*565_*566del
NM_001012270.2:c.*462_*463del	NP_001012270.1:n.*462_*463del
NM_001012271.2:c.*565_*566del	NP_001012271.1:n.*565_*566del