Canonical Allele Identifier: CA373293399
Gene: VCP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35067915C>G , CM000671.2:g.35067915C>G GRCh38
NC_000009.11:g.35067912C>G , CM000671.1:g.35067912C>G GRCh37
NC_000009.10:g.35057912C>G NCBI36
NG_007887.1:g.9828G>C , LRG_657:g.9828G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358901.11:c.278G>C MANE Select ENSP00000351777.6:p.Arg93Pro
ENST00000417448.2:c.143G>C ENSP00000399456.2:p.Arg48Pro
ENST00000448530.6:c.143G>C ENSP00000392088.2:p.Arg48Pro
ENST00000480327.2:n.550G>C
ENST00000676836.2:n.541G>C
ENST00000677257.1:c.272G>C ENSP00000504354.1:p.Arg91Pro
ENST00000678018.1:c.*249G>C ENSP00000503811.1:n.*249G>C
ENST00000678465.1:c.278G>C ENSP00000504259.1:p.Arg93Pro
ENST00000678650.1:c.143G>C ENSP00000503426.1:p.Arg48Pro
ENST00000679204.2:c.278G>C ENSP00000503131.2:p.Arg93Pro
ENST00000679449.1:c.297G>C
ENST00000679599.1:n.548G>C
ENST00000679647.1:c.278G>C ENSP00000506216.1:p.Arg93Pro
ENST00000679800.1:n.516G>C
ENST00000679862.1:c.143G>C ENSP00000504990.1:p.Arg48Pro
ENST00000679902.1:c.278G>C ENSP00000506338.1:p.Arg93Pro
ENST00000680079.1:c.*199G>C ENSP00000506523.1:n.*199G>C
ENST00000680731.1:c.143G>C ENSP00000505497.1:p.Arg48Pro
ENST00000680900.1:c.282G>C
ENST00000680916.1:c.278G>C ENSP00000505769.1:p.Arg93Pro
ENST00000681335.1:c.278G>C ENSP00000505230.1:p.Arg93Pro
ENST00000681386.1:c.143G>C ENSP00000505509.1:p.Arg48Pro
ENST00000681690.1:n.550G>C
ENST00000681845.1:c.444G>C
ENST00000358901.10:c.278G>C ENSP00000351777.6:p.Arg93Pro
ENST00000417448.1:c.143G>C ENSP00000399456.1:p.Arg48Pro
ENST00000448530.5:c.143G>C ENSP00000392088.1:p.Arg48Pro
ENST00000493886.5:n.474G>C
NM_007126.3:c.278G>C , LRG_657t1:c.278G>C NP_009057.1:p.Arg93Pro
NM_001354927.1:c.143G>C NP_001341856.1:p.Arg48Pro
NM_001354928.1:c.143G>C NP_001341857.1:p.Arg48Pro
NM_007126.4:c.278G>C NP_009057.1:p.Arg93Pro
NM_007126.5:c.278G>C MANE Select NP_009057.1:p.Arg93Pro
NM_001354927.2:c.143G>C NP_001341856.1:p.Arg48Pro
NM_001354928.2:c.143G>C NP_001341857.1:p.Arg48Pro