Canonical Allele Identifier: CA213386
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 218305
dbSNP Id: rs864309501
gnomAD v4: 9-35065274-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35065274C>T , CM000671.2:g.35065274C>T GRCh38
NC_000009.11:g.35065271C>T , CM000671.1:g.35065271C>T GRCh37
NC_000009.10:g.35055271C>T NCBI36
NG_007887.1:g.12469G>A , LRG_657:g.12469G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358901.11:c.553G>A MANE Select ENSP00000351777.6:p.Glu185Lys
ENST00000417448.2:c.418G>A ENSP00000399456.2:p.Glu140Lys
ENST00000448530.6:c.418G>A ENSP00000392088.2:p.Glu140Lys
ENST00000480327.2:n.825G>A
ENST00000676836.2:n.899G>A
ENST00000677257.1:c.547G>A ENSP00000504354.1:p.Glu183Lys
ENST00000678018.1:c.*524G>A ENSP00000503811.1:n.*524G>A
ENST00000678465.1:c.553G>A ENSP00000504259.1:p.Glu185Lys
ENST00000678650.1:c.418G>A ENSP00000503426.1:p.Glu140Lys
ENST00000679204.2:c.553G>A ENSP00000503131.2:p.Glu185Lys
ENST00000679599.1:n.823G>A
ENST00000679647.1:c.553G>A ENSP00000506216.1:p.Glu185Lys
ENST00000679800.1:n.874G>A
ENST00000679862.1:c.418G>A ENSP00000504990.1:p.Glu140Lys
ENST00000679902.1:c.553G>A ENSP00000506338.1:p.Glu185Lys
ENST00000680520.1:c.108G>A
ENST00000680731.1:c.*41G>A ENSP00000505497.1:n.*41G>A
ENST00000680834.1:c.35G>A
ENST00000680916.1:c.553G>A ENSP00000505769.1:p.Glu185Lys
ENST00000681335.1:c.553G>A ENSP00000505230.1:p.Glu185Lys
ENST00000681562.1:c.305G>A
ENST00000681690.1:n.825G>A
ENST00000681789.1:c.108G>A
ENST00000358901.10:c.553G>A ENSP00000351777.6:p.Glu185Lys
ENST00000448530.5:c.418G>A ENSP00000392088.1:p.Glu140Lys
ENST00000493886.5:n.749G>A
NM_007126.3:c.553G>A , LRG_657t1:c.553G>A NP_009057.1:p.Glu185Lys
NM_001354927.1:c.418G>A NP_001341856.1:p.Glu140Lys
NM_001354928.1:c.418G>A NP_001341857.1:p.Glu140Lys
NM_007126.4:c.553G>A NP_009057.1:p.Glu185Lys
NM_007126.5:c.553G>A MANE Select NP_009057.1:p.Glu185Lys
NM_001354927.2:c.418G>A NP_001341856.1:p.Glu140Lys
NM_001354928.2:c.418G>A NP_001341857.1:p.Glu140Lys