Canonical Allele Identifier: CA192679536

Gene: VCP

Linked Data

• ClinVar Variation Id: 1916783
• ClinVar RCV Id: RCV002590693
• dbSNP Id: rs988652510
• gnomAD v4: 9-35059225-A-G
• MyVariant Identifiers: chr9:g.35059222A>G (hg19) ; chr9:g.35059225A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35059225A>G , CM000671.2:g.35059225A>G	GRCh38
NC_000009.11:g.35059222A>G , CM000671.1:g.35059222A>G	GRCh37
NC_000009.10:g.35049222A>G	NCBI36
NG_007887.1:g.18518T>C , LRG_657:g.18518T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.2005-6T>C MANE Select	ENSP00000351777.6:n.2005-6T>C
ENST00000417448.2:c.1870-6T>C	ENSP00000399456.2:n.1870-6T>C
ENST00000448530.6:c.1870-6T>C	ENSP00000392088.2:n.1870-6T>C
ENST00000479300.2:n.533-6T>C
ENST00000676836.2:n.2748-6T>C
ENST00000677257.1:c.1999-6T>C	ENSP00000504354.1:n.1999-6T>C
ENST00000678018.1:c.*1976-6T>C	ENSP00000503811.1:n.*1976-6T>C
ENST00000678465.1:c.*1017-6T>C	ENSP00000504259.1:n.*1017-6T>C
ENST00000678650.1:c.1870-6T>C	ENSP00000503426.1:n.1870-6T>C
ENST00000679204.2:c.*646-6T>C	ENSP00000503131.2:n.*646-6T>C
ENST00000679599.1:n.3061-6T>C
ENST00000679647.1:c.2005-6T>C	ENSP00000506216.1:n.2005-6T>C
ENST00000679800.1:n.2404-6T>C
ENST00000679862.1:c.1870-6T>C	ENSP00000504990.1:n.1870-6T>C
ENST00000679902.1:c.2005-6T>C	ENSP00000506338.1:n.2005-6T>C
ENST00000680916.1:c.2055-6T>C	ENSP00000505769.1:n.2055-6T>C
ENST00000681335.1:c.2004+268T>C	ENSP00000505230.1:n.2004+268T>C
ENST00000681690.1:n.2277-6T>C
ENST00000358901.10:c.2005-6T>C	ENSP00000351777.6:n.2005-6T>C
ENST00000479300.1:n.401-6T>C
ENST00000493886.5:n.2279-6T>C
NM_007126.3:c.2005-6T>C , LRG_657t1:c.2005-6T>C	NP_009057.1:n.2005-6T>C
NM_001354927.1:c.1870-6T>C	NP_001341856.1:n.1870-6T>C
NM_001354928.1:c.1870-6T>C	NP_001341857.1:n.1870-6T>C
NM_007126.4:c.2005-6T>C	NP_009057.1:n.2005-6T>C
NM_007126.5:c.2005-6T>C MANE Select	NP_009057.1:n.2005-6T>C
NM_001354927.2:c.1870-6T>C	NP_001341856.1:n.1870-6T>C
NM_001354928.2:c.1870-6T>C	NP_001341857.1:n.1870-6T>C