Canonical Allele Identifier: CA373293559

Gene: VCP

Linked Data

• ClinVar Variation Id: 1010487
• ClinVar RCV Id: RCV001308126
• dbSNP Id: rs1828865320
• MyVariant Identifiers: chr9:g.35067925G>A (hg19) ; chr9:g.35067928G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067928G>A , CM000671.2:g.35067928G>A	GRCh38
NC_000009.11:g.35067925G>A , CM000671.1:g.35067925G>A	GRCh37
NC_000009.10:g.35057925G>A	NCBI36
NG_007887.1:g.9815C>T , LRG_657:g.9815C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.265C>T MANE Select	ENSP00000351777.6:p.Arg89Trp
ENST00000417448.2:c.130C>T	ENSP00000399456.2:p.Arg44Trp
ENST00000448530.6:c.130C>T	ENSP00000392088.2:p.Arg44Trp
ENST00000480327.2:n.537C>T
ENST00000676836.2:n.528C>T
ENST00000677257.1:c.259C>T	ENSP00000504354.1:p.Arg87Trp
ENST00000678018.1:c.*236C>T	ENSP00000503811.1:n.*236C>T
ENST00000678465.1:c.265C>T	ENSP00000504259.1:p.Arg89Trp
ENST00000678650.1:c.130C>T	ENSP00000503426.1:p.Arg44Trp
ENST00000679204.2:c.265C>T	ENSP00000503131.2:p.Arg89Trp
ENST00000679449.1:c.284C>T
ENST00000679599.1:n.535C>T
ENST00000679647.1:c.265C>T	ENSP00000506216.1:p.Arg89Trp
ENST00000679800.1:n.503C>T
ENST00000679862.1:c.130C>T	ENSP00000504990.1:p.Arg44Trp
ENST00000679902.1:c.265C>T	ENSP00000506338.1:p.Arg89Trp
ENST00000680079.1:c.*186C>T	ENSP00000506523.1:n.*186C>T
ENST00000680731.1:c.130C>T	ENSP00000505497.1:p.Arg44Trp
ENST00000680900.1:c.269C>T
ENST00000680916.1:c.265C>T	ENSP00000505769.1:p.Arg89Trp
ENST00000681335.1:c.265C>T	ENSP00000505230.1:p.Arg89Trp
ENST00000681386.1:c.130C>T	ENSP00000505509.1:p.Arg44Trp
ENST00000681690.1:n.537C>T
ENST00000681845.1:c.431C>T
ENST00000358901.10:c.265C>T	ENSP00000351777.6:p.Arg89Trp
ENST00000417448.1:c.130C>T	ENSP00000399456.1:p.Arg44Trp
ENST00000448530.5:c.130C>T	ENSP00000392088.1:p.Arg44Trp
ENST00000493886.5:n.461C>T
NM_007126.3:c.265C>T , LRG_657t1:c.265C>T	NP_009057.1:p.Arg89Trp
NM_001354927.1:c.130C>T	NP_001341856.1:p.Arg44Trp
NM_001354928.1:c.130C>T	NP_001341857.1:p.Arg44Trp
NM_007126.4:c.265C>T	NP_009057.1:p.Arg89Trp
NM_007126.5:c.265C>T MANE Select	NP_009057.1:p.Arg89Trp
NM_001354927.2:c.130C>T	NP_001341856.1:p.Arg44Trp
NM_001354928.2:c.130C>T	NP_001341857.1:p.Arg44Trp