Canonical Allele Identifier: CA373291969
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 432305
dbSNP Id: rs1554668979

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35066737C>G , CM000671.2:g.35066737C>G GRCh38
NC_000009.11:g.35066734C>G , CM000671.1:g.35066734C>G GRCh37
NC_000009.10:g.35056734C>G NCBI36
NG_007887.1:g.11006G>C , LRG_657:g.11006G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358901.11:c.383G>C MANE Select ENSP00000351777.6:p.Gly128Ala
ENST00000417448.2:c.248G>C ENSP00000399456.2:p.Gly83Ala
ENST00000448530.6:c.248G>C ENSP00000392088.2:p.Gly83Ala
ENST00000480327.2:n.655G>C
ENST00000676836.2:n.729G>C
ENST00000677257.1:c.377G>C ENSP00000504354.1:p.Gly126Ala
ENST00000678018.1:c.*354G>C ENSP00000503811.1:n.*354G>C
ENST00000678465.1:c.383G>C ENSP00000504259.1:p.Gly128Ala
ENST00000678650.1:c.248G>C ENSP00000503426.1:p.Gly83Ala
ENST00000679204.2:c.383G>C ENSP00000503131.2:p.Gly128Ala
ENST00000679599.1:n.653G>C
ENST00000679647.1:c.383G>C ENSP00000506216.1:p.Gly128Ala
ENST00000679800.1:n.704G>C
ENST00000679862.1:c.248G>C ENSP00000504990.1:p.Gly83Ala
ENST00000679902.1:c.383G>C ENSP00000506338.1:p.Gly128Ala
ENST00000680079.1:c.*304G>C ENSP00000506523.1:n.*304G>C
ENST00000680731.1:c.167+1154G>C ENSP00000505497.1:n.167+1154G>C
ENST00000680916.1:c.383G>C ENSP00000505769.1:p.Gly128Ala
ENST00000681335.1:c.383G>C ENSP00000505230.1:p.Gly128Ala
ENST00000681562.1:c.81G>C
ENST00000681690.1:n.655G>C
ENST00000681845.1:c.549G>C
ENST00000358901.10:c.383G>C ENSP00000351777.6:p.Gly128Ala
ENST00000417448.1:c.248G>C ENSP00000399456.1:p.Gly83Ala
ENST00000448530.5:c.248G>C ENSP00000392088.1:p.Gly83Ala
ENST00000493886.5:n.579G>C
NM_007126.3:c.383G>C , LRG_657t1:c.383G>C NP_009057.1:p.Gly128Ala
NM_001354927.1:c.248G>C NP_001341856.1:p.Gly83Ala
NM_001354928.1:c.248G>C NP_001341857.1:p.Gly83Ala
NM_007126.4:c.383G>C NP_009057.1:p.Gly128Ala
NM_007126.5:c.383G>C MANE Select NP_009057.1:p.Gly128Ala
NM_001354927.2:c.248G>C NP_001341856.1:p.Gly83Ala
NM_001354928.2:c.248G>C NP_001341857.1:p.Gly83Ala