Canonical Allele Identifier: CA277489

Gene: VCP

Linked Data

• ClinVar Variation Id: 217028
• ClinVar RCV Id: RCV000196145 ; RCV000494556 ; RCV002229498
• dbSNP Id: rs121909330
• MyVariant Identifiers: chr9:g.35065361G>C (hg19) ; chr9:g.35065364G>C (hg38)
• PubMed: PMID:25326637

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.463C>G MANE Select	ENSP00000351777.6:p.Arg155Gly
ENST00000417448.2:c.328C>G	ENSP00000399456.2:p.Arg110Gly
ENST00000448530.6:c.328C>G	ENSP00000392088.2:p.Arg110Gly
ENST00000480327.2:n.735C>G
ENST00000676836.2:n.809C>G
ENST00000677257.1:c.457C>G	ENSP00000504354.1:p.Arg153Gly
ENST00000678018.1:c.*434C>G	ENSP00000503811.1:n.*434C>G
ENST00000678465.1:c.463C>G	ENSP00000504259.1:p.Arg155Gly
ENST00000678650.1:c.328C>G	ENSP00000503426.1:p.Arg110Gly
ENST00000679204.2:c.463C>G	ENSP00000503131.2:p.Arg155Gly
ENST00000679599.1:n.733C>G
ENST00000679647.1:c.463C>G	ENSP00000506216.1:p.Arg155Gly
ENST00000679800.1:n.784C>G
ENST00000679862.1:c.328C>G	ENSP00000504990.1:p.Arg110Gly
ENST00000679902.1:c.463C>G	ENSP00000506338.1:p.Arg155Gly
ENST00000680520.1:c.18C>G
ENST00000680731.1:c.185C>G	ENSP00000505497.1:p.Pro62Arg
ENST00000680916.1:c.463C>G	ENSP00000505769.1:p.Arg155Gly
ENST00000681335.1:c.463C>G	ENSP00000505230.1:p.Arg155Gly
ENST00000681562.1:c.215C>G
ENST00000681690.1:n.735C>G
ENST00000681789.1:c.18C>G
ENST00000681845.1:c.629C>G
ENST00000358901.10:c.463C>G	ENSP00000351777.6:p.Arg155Gly
ENST00000417448.1:c.328C>G	ENSP00000399456.1:p.Arg110Gly
ENST00000448530.5:c.328C>G	ENSP00000392088.1:p.Arg110Gly
ENST00000493886.5:n.659C>G
NM_007126.3:c.463C>G , LRG_657t1:c.463C>G	NP_009057.1:p.Arg155Gly
NM_001354927.1:c.328C>G	NP_001341856.1:p.Arg110Gly
NM_001354928.1:c.328C>G	NP_001341857.1:p.Arg110Gly
NM_007126.4:c.463C>G	NP_009057.1:p.Arg155Gly
NM_007126.5:c.463C>G MANE Select	NP_009057.1:p.Arg155Gly
NM_001354927.2:c.328C>G	NP_001341856.1:p.Arg110Gly
NM_001354928.2:c.328C>G	NP_001341857.1:p.Arg110Gly