Canonical Allele Identifier: CA464602500

Gene: VCP

Linked Data

• ClinVar Variation Id: 2953112
• ClinVar RCV Id: RCV003810230
• dbSNP Id: rs1373925196
• gnomAD v4: 9-35068025-T-C
• MyVariant Identifiers: chr9:g.35068022T>C (hg19) ; chr9:g.35068025T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068025T>C , CM000671.2:g.35068025T>C	GRCh38
NC_000009.11:g.35068022T>C , CM000671.1:g.35068022T>C	GRCh37
NC_000009.10:g.35058022T>C	NCBI36
NG_007887.1:g.9718A>G , LRG_657:g.9718A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.168A>G MANE Select	ENSP00000351777.6:p.Thr56=
ENST00000417448.2:c.33A>G	ENSP00000399456.2:p.Thr11=
ENST00000448530.6:c.33A>G	ENSP00000392088.2:p.Thr11=
ENST00000480327.2:n.440A>G
ENST00000676836.2:n.431A>G
ENST00000677257.1:c.162A>G	ENSP00000504354.1:p.Thr54=
ENST00000678018.1:c.*139A>G	ENSP00000503811.1:n.*139A>G
ENST00000678465.1:c.168A>G	ENSP00000504259.1:p.Thr56=
ENST00000678650.1:c.33A>G	ENSP00000503426.1:p.Thr11=
ENST00000679204.2:c.168A>G	ENSP00000503131.2:p.Thr56=
ENST00000679449.1:c.187A>G
ENST00000679599.1:n.438A>G
ENST00000679647.1:c.168A>G	ENSP00000506216.1:p.Thr56=
ENST00000679800.1:n.406A>G
ENST00000679862.1:c.33A>G	ENSP00000504990.1:p.Thr11=
ENST00000679902.1:c.168A>G	ENSP00000506338.1:p.Thr56=
ENST00000680079.1:c.*89A>G	ENSP00000506523.1:n.*89A>G
ENST00000680731.1:c.33A>G	ENSP00000505497.1:p.Thr11=
ENST00000680900.1:c.172A>G
ENST00000680916.1:c.168A>G	ENSP00000505769.1:p.Thr56=
ENST00000681335.1:c.168A>G	ENSP00000505230.1:p.Thr56=
ENST00000681386.1:c.33A>G	ENSP00000505509.1:p.Thr11=
ENST00000681690.1:n.440A>G
ENST00000681845.1:c.334A>G
ENST00000358901.10:c.168A>G	ENSP00000351777.6:p.Thr56=
ENST00000417448.1:c.33A>G	ENSP00000399456.1:p.Thr11=
ENST00000448530.5:c.33A>G	ENSP00000392088.1:p.Thr11=
ENST00000493886.5:n.364A>G
NM_007126.3:c.168A>G , LRG_657t1:c.168A>G	NP_009057.1:p.Thr56=
NM_001354927.1:c.33A>G	NP_001341856.1:p.Thr11=
NM_001354928.1:c.33A>G	NP_001341857.1:p.Thr11=
NM_007126.4:c.168A>G	NP_009057.1:p.Thr56=
NM_007126.5:c.168A>G MANE Select	NP_009057.1:p.Thr56=
NM_001354927.2:c.33A>G	NP_001341856.1:p.Thr11=
NM_001354928.2:c.33A>G	NP_001341857.1:p.Thr11=