Canonical Allele Identifier: CA986568428

Gene: BIRC5

Linked Data

• gnomAD v3: 17-78224064-G-GTTTTTTTTTT
• gnomAD v4: 17-78224064-G-GTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224068_78224077dup , CM000679.2:g.78224068_78224077dup	GRCh38
NC_000017.10:g.76220149_76220158dup , CM000679.1:g.76220149_76220158dup	GRCh37
NC_000017.9:g.73731744_73731753dup	NCBI36
NG_029069.1:g.14873_14882dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*514_*523dup MANE Select	ENSP00000324180.4:n.*514_*523dup
ENST00000301633.8:c.*514_*523dup	ENSP00000301633.3:n.*514_*523dup
ENST00000350051.7:c.*514_*523dup	ENSP00000324180.4:n.*514_*523dup
ENST00000374948.6:c.*411_*420dup	ENSP00000364086.1:n.*411_*420dup
NM_001012270.1:c.*411_*420dup	NP_001012270.1:n.*411_*420dup
NM_001012271.1:c.*514_*523dup	NP_001012271.1:n.*514_*523dup
NM_001168.2:c.*514_*523dup	NP_001159.2:n.*514_*523dup
XR_243654.3:n.1145_1154dup
XR_934452.1:n.1214_1223dup
XR_243654.5:n.1145_1154dup
XR_934452.3:n.1214_1223dup
NM_001168.3:c.*514_*523dup MANE Select	NP_001159.2:n.*514_*523dup
NM_001012270.2:c.*411_*420dup	NP_001012270.1:n.*411_*420dup
NM_001012271.2:c.*514_*523dup	NP_001012271.1:n.*514_*523dup