Canonical Allele Identifier: CA656884491

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78224064-GTTT-G
• COSMIC: COSN15657316

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224075_78224077del , CM000679.2:g.78224075_78224077del	GRCh38
NC_000017.10:g.76220156_76220158del , CM000679.1:g.76220156_76220158del	GRCh37
NC_000017.9:g.73731751_73731753del	NCBI36
NG_029069.1:g.14880_14882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*521_*523del MANE Select	ENSP00000324180.4:n.*521_*523del
ENST00000301633.8:c.*521_*523del	ENSP00000301633.3:n.*521_*523del
ENST00000350051.7:c.*521_*523del	ENSP00000324180.4:n.*521_*523del
ENST00000374948.6:c.*418_*420del	ENSP00000364086.1:n.*418_*420del
NM_001012270.1:c.*418_*420del	NP_001012270.1:n.*418_*420del
NM_001012271.1:c.*521_*523del	NP_001012271.1:n.*521_*523del
NM_001168.2:c.*521_*523del	NP_001159.2:n.*521_*523del
XR_243654.3:n.1152_1154del
XR_934452.1:n.1221_1223del
XR_243654.5:n.1152_1154del
XR_934452.3:n.1221_1223del
NM_001168.3:c.*521_*523del MANE Select	NP_001159.2:n.*521_*523del
NM_001012270.2:c.*418_*420del	NP_001012270.1:n.*418_*420del
NM_001012271.2:c.*521_*523del	NP_001012271.1:n.*521_*523del