Canonical Allele Identifier: CA587237079
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1591848
ClinVar RCV Id: RCV002096398
dbSNP Id: rs1401092893
gnomAD v2: 9-35059806-A-G
gnomAD v3: 9-35059809-A-G
gnomAD v4: 9-35059809-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35059809A>G , CM000671.2:g.35059809A>G GRCh38
NC_000009.11:g.35059806A>G , CM000671.1:g.35059806A>G GRCh37
NC_000009.10:g.35049806A>G NCBI36
NG_007887.1:g.17934T>C , LRG_657:g.17934T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358901.11:c.1696-8T>C MANE Select ENSP00000351777.6:n.1696-8T>C
ENST00000417448.2:c.1561-8T>C ENSP00000399456.2:n.1561-8T>C
ENST00000448530.6:c.1561-8T>C ENSP00000392088.2:n.1561-8T>C
ENST00000479300.2:n.216T>C
ENST00000480327.2:n.2109-8T>C
ENST00000676836.2:n.2439-8T>C
ENST00000677257.1:c.1690-8T>C ENSP00000504354.1:n.1690-8T>C
ENST00000678018.1:c.*1667-8T>C ENSP00000503811.1:n.*1667-8T>C
ENST00000678465.1:c.*708-8T>C ENSP00000504259.1:n.*708-8T>C
ENST00000678650.1:c.1561-8T>C ENSP00000503426.1:n.1561-8T>C
ENST00000679204.2:c.*337-8T>C ENSP00000503131.2:n.*337-8T>C
ENST00000679599.1:n.2744T>C
ENST00000679647.1:c.1696-8T>C ENSP00000506216.1:n.1696-8T>C
ENST00000679800.1:n.2095-8T>C
ENST00000679862.1:c.1561-8T>C ENSP00000504990.1:n.1561-8T>C
ENST00000679902.1:c.1696-8T>C ENSP00000506338.1:n.1696-8T>C
ENST00000680916.1:c.1696-8T>C ENSP00000505769.1:n.1696-8T>C
ENST00000681335.1:c.1696-8T>C ENSP00000505230.1:n.1696-8T>C
ENST00000681690.1:n.1968-8T>C
ENST00000358901.10:c.1696-8T>C ENSP00000351777.6:n.1696-8T>C
ENST00000479300.1:n.84T>C
ENST00000480327.1:n.831-8T>C
ENST00000493886.5:n.1970-8T>C
NM_007126.3:c.1696-8T>C , LRG_657t1:c.1696-8T>C NP_009057.1:n.1696-8T>C
NM_001354927.1:c.1561-8T>C NP_001341856.1:n.1561-8T>C
NM_001354928.1:c.1561-8T>C NP_001341857.1:n.1561-8T>C
NM_007126.4:c.1696-8T>C NP_009057.1:n.1696-8T>C
NM_007126.5:c.1696-8T>C MANE Select NP_009057.1:n.1696-8T>C
NM_001354927.2:c.1561-8T>C NP_001341856.1:n.1561-8T>C
NM_001354928.2:c.1561-8T>C NP_001341857.1:n.1561-8T>C