Canonical Allele Identifier: CA254398

Gene: VCP

Linked Data

• ClinVar Variation Id: 8469
• ClinVar RCV Id: RCV000008990 ; RCV000372207 ; RCV000685660 ; RCV001095424
• dbSNP Id: rs121909330
• COSMIC: COSM3657096
• MyVariant Identifiers: chr9:g.35065361G>A (hg19) ; chr9:g.35065364G>A (hg38)
• PubMed: PMID:15034582 ; PMID:16790606 ; PMID:19237541 ; PMID:21320982

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35065364G>A , CM000671.2:g.35065364G>A	GRCh38
NC_000009.11:g.35065361G>A , CM000671.1:g.35065361G>A	GRCh37
NC_000009.10:g.35055361G>A	NCBI36
NG_007887.1:g.12379C>T , LRG_657:g.12379C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.463C>T MANE Select	ENSP00000351777.6:p.Arg155Cys
ENST00000417448.2:c.328C>T	ENSP00000399456.2:p.Arg110Cys
ENST00000448530.6:c.328C>T	ENSP00000392088.2:p.Arg110Cys
ENST00000480327.2:n.735C>T
ENST00000676836.2:n.809C>T
ENST00000677257.1:c.457C>T	ENSP00000504354.1:p.Arg153Cys
ENST00000678018.1:c.*434C>T	ENSP00000503811.1:n.*434C>T
ENST00000678465.1:c.463C>T	ENSP00000504259.1:p.Arg155Cys
ENST00000678650.1:c.328C>T	ENSP00000503426.1:p.Arg110Cys
ENST00000679204.2:c.463C>T	ENSP00000503131.2:p.Arg155Cys
ENST00000679599.1:n.733C>T
ENST00000679647.1:c.463C>T	ENSP00000506216.1:p.Arg155Cys
ENST00000679800.1:n.784C>T
ENST00000679862.1:c.328C>T	ENSP00000504990.1:p.Arg110Cys
ENST00000679902.1:c.463C>T	ENSP00000506338.1:p.Arg155Cys
ENST00000680520.1:c.18C>T
ENST00000680731.1:c.185C>T	ENSP00000505497.1:p.Pro62Leu
ENST00000680916.1:c.463C>T	ENSP00000505769.1:p.Arg155Cys
ENST00000681335.1:c.463C>T	ENSP00000505230.1:p.Arg155Cys
ENST00000681562.1:c.215C>T
ENST00000681690.1:n.735C>T
ENST00000681789.1:c.18C>T
ENST00000681845.1:c.629C>T
ENST00000358901.10:c.463C>T	ENSP00000351777.6:p.Arg155Cys
ENST00000417448.1:c.328C>T	ENSP00000399456.1:p.Arg110Cys
ENST00000448530.5:c.328C>T	ENSP00000392088.1:p.Arg110Cys
ENST00000493886.5:n.659C>T
NM_007126.3:c.463C>T , LRG_657t1:c.463C>T	NP_009057.1:p.Arg155Cys
NM_001354927.1:c.328C>T	NP_001341856.1:p.Arg110Cys
NM_001354928.1:c.328C>T	NP_001341857.1:p.Arg110Cys
NM_007126.4:c.463C>T	NP_009057.1:p.Arg155Cys
NM_007126.5:c.463C>T MANE Select	NP_009057.1:p.Arg155Cys
NM_001354927.2:c.328C>T	NP_001341856.1:p.Arg110Cys
NM_001354928.2:c.328C>T	NP_001341857.1:p.Arg110Cys