Canonical Allele Identifier: CA128985

Gene: VCP

Linked Data

• ClinVar Variation Id: 30153
• ClinVar RCV Id: RCV000023066
• dbSNP Id: rs387906790
• gnomAD v2: 9-35059720-C-T
• MyVariant Identifiers: chr9:g.35059720C>T (hg19) ; chr9:g.35059723C>T (hg38)
• PubMed: PMID:21145000

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35059723C>T , CM000671.2:g.35059723C>T	GRCh38
NC_000009.11:g.35059720C>T , CM000671.1:g.35059720C>T	GRCh37
NC_000009.10:g.35049720C>T	NCBI36
NG_007887.1:g.18020G>A , LRG_657:g.18020G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.1774G>A MANE Select	ENSP00000351777.6:p.Asp592Asn
ENST00000417448.2:c.1639G>A	ENSP00000399456.2:p.Asp547Asn
ENST00000448530.6:c.1639G>A	ENSP00000392088.2:p.Asp547Asn
ENST00000479300.2:n.302G>A
ENST00000676836.2:n.2517G>A
ENST00000677257.1:c.1768G>A	ENSP00000504354.1:p.Asp590Asn
ENST00000678018.1:c.*1745G>A	ENSP00000503811.1:n.*1745G>A
ENST00000678465.1:c.*786G>A	ENSP00000504259.1:n.*786G>A
ENST00000678650.1:c.1639G>A	ENSP00000503426.1:p.Asp547Asn
ENST00000679204.2:c.*415G>A	ENSP00000503131.2:n.*415G>A
ENST00000679599.1:n.2830G>A
ENST00000679647.1:c.1774G>A	ENSP00000506216.1:p.Asp592Asn
ENST00000679800.1:n.2173G>A
ENST00000679862.1:c.1639G>A	ENSP00000504990.1:p.Asp547Asn
ENST00000679902.1:c.1774G>A	ENSP00000506338.1:p.Asp592Asn
ENST00000680916.1:c.1774G>A	ENSP00000505769.1:p.Asp592Asn
ENST00000681335.1:c.1774G>A	ENSP00000505230.1:p.Asp592Asn
ENST00000681690.1:n.2046G>A
ENST00000358901.10:c.1774G>A	ENSP00000351777.6:p.Asp592Asn
ENST00000479300.1:n.170G>A
ENST00000493886.5:n.2048G>A
NM_007126.3:c.1774G>A , LRG_657t1:c.1774G>A	NP_009057.1:p.Asp592Asn
NM_001354927.1:c.1639G>A	NP_001341856.1:p.Asp547Asn
NM_001354928.1:c.1639G>A	NP_001341857.1:p.Asp547Asn
NM_007126.4:c.1774G>A	NP_009057.1:p.Asp592Asn
NM_007126.5:c.1774G>A MANE Select	NP_009057.1:p.Asp592Asn
NM_001354927.2:c.1639G>A	NP_001341856.1:p.Asp547Asn
NM_001354928.2:c.1639G>A	NP_001341857.1:p.Asp547Asn