Canonical Allele Identifier: CA5039564

Gene: VCP

Linked Data

• ClinVar Variation Id: 366721
• ClinVar RCV Id: RCV000293440 ; RCV000338806 ; RCV000548347 ; RCV001086142 ; RCV001699407
• dbSNP Id: rs114256093
• ExAC: 9:35068364 A / G
• gnomAD v2: 9-35068364-A-G
• gnomAD v3: 9-35068367-A-G
• gnomAD v4: 9-35068367-A-G
• MyVariant Identifiers: chr9:g.35068364A>G (hg19) ; chr9:g.35068367A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068367A>G , CM000671.2:g.35068367A>G	GRCh38
NC_000009.11:g.35068364A>G , CM000671.1:g.35068364A>G	GRCh37
NC_000009.10:g.35058364A>G	NCBI36
NG_007887.1:g.9376T>C , LRG_657:g.9376T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.18-5T>C MANE Select	ENSP00000351777.6:n.18-5T>C
ENST00000417448.2:c.-118-5T>C	ENSP00000399456.2:n.-118-5T>C
ENST00000448530.6:c.-118-5T>C	ENSP00000392088.2:n.-118-5T>C
ENST00000480327.2:n.290-5T>C
ENST00000676836.2:n.281-5T>C
ENST00000677257.1:c.18-5T>C	ENSP00000504354.1:n.18-5T>C
ENST00000678018.1:c.18-5T>C	ENSP00000503811.1:n.18-5T>C
ENST00000678465.1:c.18-5T>C	ENSP00000504259.1:n.18-5T>C
ENST00000678650.1:c.-110-13T>C	ENSP00000503426.1:n.-110-13T>C
ENST00000679204.2:c.18-5T>C	ENSP00000503131.2:n.18-5T>C
ENST00000679392.1:n.160-5T>C
ENST00000679599.1:n.288-5T>C
ENST00000679647.1:c.18-5T>C	ENSP00000506216.1:n.18-5T>C
ENST00000679800.1:n.256-5T>C
ENST00000679862.1:c.-118-5T>C	ENSP00000504990.1:n.-118-5T>C
ENST00000679901.1:n.347-5T>C
ENST00000679902.1:c.18-5T>C	ENSP00000506338.1:n.18-5T>C
ENST00000680079.1:c.110-5T>C	ENSP00000506523.1:n.110-5T>C
ENST00000680108.1:n.304-5T>C
ENST00000680575.1:n.399-5T>C
ENST00000680916.1:c.18-5T>C	ENSP00000505769.1:n.18-5T>C
ENST00000681335.1:c.18-5T>C	ENSP00000505230.1:n.18-5T>C
ENST00000681386.1:c.-6-304T>C	ENSP00000505509.1:n.-6-304T>C
ENST00000681690.1:n.290-5T>C
ENST00000681845.1:c.184-5T>C
ENST00000358901.10:c.18-5T>C	ENSP00000351777.6:n.18-5T>C
ENST00000417448.1:c.-118-5T>C	ENSP00000399456.1:n.-118-5T>C
ENST00000448530.5:c.-118-5T>C	ENSP00000392088.1:n.-118-5T>C
ENST00000493886.5:n.214-5T>C
NM_007126.3:c.18-5T>C , LRG_657t1:c.18-5T>C	NP_009057.1:n.18-5T>C
NM_001354927.1:c.-118-5T>C	NP_001341856.1:n.-118-5T>C
NM_001354928.1:c.-118-5T>C	NP_001341857.1:n.-118-5T>C
NM_007126.4:c.18-5T>C	NP_009057.1:n.18-5T>C
NM_007126.5:c.18-5T>C MANE Select	NP_009057.1:n.18-5T>C
NM_001354927.2:c.-118-5T>C	NP_001341856.1:n.-118-5T>C
NM_001354928.2:c.-118-5T>C	NP_001341857.1:n.-118-5T>C