Canonical Allele Identifier: CA2276860777

Gene: BIRC5

Linked Data

• dbSNP Id: rs2076534422

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224107_78224108del , CM000679.2:g.78224107_78224108del	GRCh38
NC_000017.10:g.76220188_76220189del , CM000679.1:g.76220188_76220189del	GRCh37
NC_000017.9:g.73731783_73731784del	NCBI36
NG_029069.1:g.14912_14913del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*553_*554del MANE Select	ENSP00000324180.4:n.*553_*554del
ENST00000301633.8:c.*553_*554del	ENSP00000301633.3:n.*553_*554del
ENST00000350051.7:c.*553_*554del	ENSP00000324180.4:n.*553_*554del
ENST00000374948.6:c.*450_*451del	ENSP00000364086.1:n.*450_*451del
NM_001012270.1:c.*450_*451del	NP_001012270.1:n.*450_*451del
NM_001012271.1:c.*553_*554del	NP_001012271.1:n.*553_*554del
NM_001168.2:c.*553_*554del	NP_001159.2:n.*553_*554del
XR_243654.3:n.1184_1185del
XR_934452.1:n.1253_1254del
XR_243654.5:n.1184_1185del
XR_934452.3:n.1253_1254del
NM_001168.3:c.*553_*554del MANE Select	NP_001159.2:n.*553_*554del
NM_001012270.2:c.*450_*451del	NP_001012270.1:n.*450_*451del
NM_001012271.2:c.*553_*554del	NP_001012271.1:n.*553_*554del