Canonical Allele Identifier: CA254402

Gene: VCP

Linked Data

• ClinVar Variation Id: 8471
• ClinVar RCV Id: RCV000008992
• dbSNP Id: rs121909332
• MyVariant Identifiers: chr9:g.35067907G>C (hg19) ; chr9:g.35067910G>C (hg38)
• PubMed: PMID:15034582 ; PMID:16321991

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067910G>C , CM000671.2:g.35067910G>C	GRCh38
NC_000009.11:g.35067907G>C , CM000671.1:g.35067907G>C	GRCh37
NC_000009.10:g.35057907G>C	NCBI36
NG_007887.1:g.9833C>G , LRG_657:g.9833C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.283C>G MANE Select	ENSP00000351777.6:p.Arg95Gly
ENST00000417448.2:c.148C>G	ENSP00000399456.2:p.Arg50Gly
ENST00000448530.6:c.148C>G	ENSP00000392088.2:p.Arg50Gly
ENST00000480327.2:n.555C>G
ENST00000676836.2:n.546C>G
ENST00000677257.1:c.277C>G	ENSP00000504354.1:p.Arg93Gly
ENST00000678018.1:c.*254C>G	ENSP00000503811.1:n.*254C>G
ENST00000678465.1:c.283C>G	ENSP00000504259.1:p.Arg95Gly
ENST00000678650.1:c.148C>G	ENSP00000503426.1:p.Arg50Gly
ENST00000679204.2:c.283C>G	ENSP00000503131.2:p.Arg95Gly
ENST00000679449.1:c.302C>G
ENST00000679599.1:n.553C>G
ENST00000679647.1:c.283C>G	ENSP00000506216.1:p.Arg95Gly
ENST00000679800.1:n.521C>G
ENST00000679862.1:c.148C>G	ENSP00000504990.1:p.Arg50Gly
ENST00000679902.1:c.283C>G	ENSP00000506338.1:p.Arg95Gly
ENST00000680079.1:c.*204C>G	ENSP00000506523.1:n.*204C>G
ENST00000680731.1:c.148C>G	ENSP00000505497.1:p.Arg50Gly
ENST00000680900.1:c.287C>G
ENST00000680916.1:c.283C>G	ENSP00000505769.1:p.Arg95Gly
ENST00000681335.1:c.283C>G	ENSP00000505230.1:p.Arg95Gly
ENST00000681386.1:c.148C>G	ENSP00000505509.1:p.Arg50Gly
ENST00000681690.1:n.555C>G
ENST00000681845.1:c.449C>G
ENST00000358901.10:c.283C>G	ENSP00000351777.6:p.Arg95Gly
ENST00000417448.1:c.148C>G	ENSP00000399456.1:p.Arg50Gly
ENST00000448530.5:c.148C>G	ENSP00000392088.1:p.Arg50Gly
ENST00000493886.5:n.479C>G
NM_007126.3:c.283C>G , LRG_657t1:c.283C>G	NP_009057.1:p.Arg95Gly
NM_001354927.1:c.148C>G	NP_001341856.1:p.Arg50Gly
NM_001354928.1:c.148C>G	NP_001341857.1:p.Arg50Gly
NM_007126.4:c.283C>G	NP_009057.1:p.Arg95Gly
NM_007126.5:c.283C>G MANE Select	NP_009057.1:p.Arg95Gly
NM_001354927.2:c.148C>G	NP_001341856.1:p.Arg50Gly
NM_001354928.2:c.148C>G	NP_001341857.1:p.Arg50Gly