Canonical Allele Identifier: CA2810526046

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224056_78224069del , CM000679.2:g.78224056_78224069del	GRCh38
NC_000017.10:g.76220137_76220150del , CM000679.1:g.76220137_76220150del	GRCh37
NC_000017.9:g.73731732_73731745del	NCBI36
NG_029069.1:g.14861_14874del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*502_*515del MANE Select	ENSP00000324180.4:n.*502_*515del
ENST00000301633.8:c.*502_*515del	ENSP00000301633.3:n.*502_*515del
ENST00000350051.7:c.*502_*515del	ENSP00000324180.4:n.*502_*515del
ENST00000374948.6:c.*399_*412del	ENSP00000364086.1:n.*399_*412del
NM_001012270.1:c.*399_*412del	NP_001012270.1:n.*399_*412del
NM_001012271.1:c.*502_*515del	NP_001012271.1:n.*502_*515del
NM_001168.2:c.*502_*515del	NP_001159.2:n.*502_*515del
XR_243654.3:n.1133_1146del
XR_934452.1:n.1202_1215del
XR_243654.5:n.1133_1146del
XR_934452.3:n.1202_1215del
NM_001168.3:c.*502_*515del MANE Select	NP_001159.2:n.*502_*515del
NM_001012270.2:c.*399_*412del	NP_001012270.1:n.*399_*412del
NM_001012271.2:c.*502_*515del	NP_001012271.1:n.*502_*515del