Canonical Allele Identifier: CA373276541

Gene: VCP

Linked Data

• ClinVar Variation Id: 1359439
• ClinVar RCV Id: RCV001864719
• dbSNP Id: rs1255802734
• gnomAD v2: 9-35059726-T-C
• gnomAD v4: 9-35059729-T-C
• MyVariant Identifiers: chr9:g.35059726T>C (hg19) ; chr9:g.35059729T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35059729T>C , CM000671.2:g.35059729T>C	GRCh38
NC_000009.11:g.35059726T>C , CM000671.1:g.35059726T>C	GRCh37
NC_000009.10:g.35049726T>C	NCBI36
NG_007887.1:g.18014A>G , LRG_657:g.18014A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.1768A>G MANE Select	ENSP00000351777.6:p.Ile590Val
ENST00000417448.2:c.1633A>G	ENSP00000399456.2:p.Ile545Val
ENST00000448530.6:c.1633A>G	ENSP00000392088.2:p.Ile545Val
ENST00000479300.2:n.296A>G
ENST00000676836.2:n.2511A>G
ENST00000677257.1:c.1762A>G	ENSP00000504354.1:p.Ile588Val
ENST00000678018.1:c.*1739A>G	ENSP00000503811.1:n.*1739A>G
ENST00000678465.1:c.*780A>G	ENSP00000504259.1:n.*780A>G
ENST00000678650.1:c.1633A>G	ENSP00000503426.1:p.Ile545Val
ENST00000679204.2:c.*409A>G	ENSP00000503131.2:n.*409A>G
ENST00000679599.1:n.2824A>G
ENST00000679647.1:c.1768A>G	ENSP00000506216.1:p.Ile590Val
ENST00000679800.1:n.2167A>G
ENST00000679862.1:c.1633A>G	ENSP00000504990.1:p.Ile545Val
ENST00000679902.1:c.1768A>G	ENSP00000506338.1:p.Ile590Val
ENST00000680916.1:c.1768A>G	ENSP00000505769.1:p.Ile590Val
ENST00000681335.1:c.1768A>G	ENSP00000505230.1:p.Ile590Val
ENST00000681690.1:n.2040A>G
ENST00000358901.10:c.1768A>G	ENSP00000351777.6:p.Ile590Val
ENST00000479300.1:n.164A>G
ENST00000493886.5:n.2042A>G
NM_007126.3:c.1768A>G , LRG_657t1:c.1768A>G	NP_009057.1:p.Ile590Val
NM_001354927.1:c.1633A>G	NP_001341856.1:p.Ile545Val
NM_001354928.1:c.1633A>G	NP_001341857.1:p.Ile545Val
NM_007126.4:c.1768A>G	NP_009057.1:p.Ile590Val
NM_007126.5:c.1768A>G MANE Select	NP_009057.1:p.Ile590Val
NM_001354927.2:c.1633A>G	NP_001341856.1:p.Ile545Val
NM_001354928.2:c.1633A>G	NP_001341857.1:p.Ile545Val