Canonical Allele Identifier: CA5039169

Gene: VCP

Linked Data

• ClinVar Variation Id: 501835
• ClinVar RCV Id: RCV000598527 ; RCV001403231 ; RCV002413682 ; RCV004530715
• dbSNP Id: rs141275388
• ExAC: 9:35059598 G / T
• gnomAD v2: 9-35059598-G-T
• gnomAD v3: 9-35059601-G-T
• gnomAD v4: 9-35059601-G-T
• MyVariant Identifiers: chr9:g.35059598G>T (hg19) ; chr9:g.35059601G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35059601G>T , CM000671.2:g.35059601G>T	GRCh38
NC_000009.11:g.35059598G>T , CM000671.1:g.35059598G>T	GRCh37
NC_000009.10:g.35049598G>T	NCBI36
NG_007887.1:g.18142C>A , LRG_657:g.18142C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.1896C>A MANE Select	ENSP00000351777.6:p.Ala632=
ENST00000417448.2:c.1761C>A	ENSP00000399456.2:p.Ala587=
ENST00000448530.6:c.1761C>A	ENSP00000392088.2:p.Ala587=
ENST00000479300.2:n.424C>A
ENST00000676836.2:n.2639C>A
ENST00000677257.1:c.1890C>A	ENSP00000504354.1:p.Ala630=
ENST00000678018.1:c.*1867C>A	ENSP00000503811.1:n.*1867C>A
ENST00000678465.1:c.*908C>A	ENSP00000504259.1:n.*908C>A
ENST00000678650.1:c.1761C>A	ENSP00000503426.1:p.Ala587=
ENST00000679204.2:c.*537C>A	ENSP00000503131.2:n.*537C>A
ENST00000679599.1:n.2952C>A
ENST00000679647.1:c.1896C>A	ENSP00000506216.1:p.Ala632=
ENST00000679800.1:n.2295C>A
ENST00000679862.1:c.1761C>A	ENSP00000504990.1:p.Ala587=
ENST00000679902.1:c.1896C>A	ENSP00000506338.1:p.Ala632=
ENST00000680916.1:c.1896C>A	ENSP00000505769.1:p.Ala632=
ENST00000681335.1:c.1896C>A	ENSP00000505230.1:p.Ala632=
ENST00000681690.1:n.2168C>A
ENST00000358901.10:c.1896C>A	ENSP00000351777.6:p.Ala632=
ENST00000479300.1:n.292C>A
ENST00000493886.5:n.2170C>A
NM_007126.3:c.1896C>A , LRG_657t1:c.1896C>A	NP_009057.1:p.Ala632=
NM_001354927.1:c.1761C>A	NP_001341856.1:p.Ala587=
NM_001354928.1:c.1761C>A	NP_001341857.1:p.Ala587=
NM_007126.4:c.1896C>A	NP_009057.1:p.Ala632=
NM_007126.5:c.1896C>A MANE Select	NP_009057.1:p.Ala632=
NM_001354927.2:c.1761C>A	NP_001341856.1:p.Ala587=
NM_001354928.2:c.1761C>A	NP_001341857.1:p.Ala587=