Canonical Allele Identifier: CA464602494
Gene: VCP HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.35068019C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35068022C>G , CM000671.2:g.35068022C>G GRCh38
NC_000009.11:g.35068019C>G , CM000671.1:g.35068019C>G GRCh37
NC_000009.10:g.35058019C>G NCBI36
NG_007887.1:g.9721G>C , LRG_657:g.9721G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358901.11:c.171G>C MANE Select ENSP00000351777.6:p.Val57=
ENST00000417448.2:c.36G>C ENSP00000399456.2:p.Val12=
ENST00000448530.6:c.36G>C ENSP00000392088.2:p.Val12=
ENST00000480327.2:n.443G>C
ENST00000676836.2:n.434G>C
ENST00000677257.1:c.165G>C ENSP00000504354.1:p.Val55=
ENST00000678018.1:c.*142G>C ENSP00000503811.1:n.*142G>C
ENST00000678465.1:c.171G>C ENSP00000504259.1:p.Val57=
ENST00000678650.1:c.36G>C ENSP00000503426.1:p.Val12=
ENST00000679204.2:c.171G>C ENSP00000503131.2:p.Val57=
ENST00000679449.1:c.190G>C
ENST00000679599.1:n.441G>C
ENST00000679647.1:c.171G>C ENSP00000506216.1:p.Val57=
ENST00000679800.1:n.409G>C
ENST00000679862.1:c.36G>C ENSP00000504990.1:p.Val12=
ENST00000679902.1:c.171G>C ENSP00000506338.1:p.Val57=
ENST00000680079.1:c.*92G>C ENSP00000506523.1:n.*92G>C
ENST00000680731.1:c.36G>C ENSP00000505497.1:p.Val12=
ENST00000680900.1:c.175G>C
ENST00000680916.1:c.171G>C ENSP00000505769.1:p.Val57=
ENST00000681335.1:c.171G>C ENSP00000505230.1:p.Val57=
ENST00000681386.1:c.36G>C ENSP00000505509.1:p.Val12=
ENST00000681690.1:n.443G>C
ENST00000681845.1:c.337G>C
ENST00000358901.10:c.171G>C ENSP00000351777.6:p.Val57=
ENST00000417448.1:c.36G>C ENSP00000399456.1:p.Val12=
ENST00000448530.5:c.36G>C ENSP00000392088.1:p.Val12=
ENST00000493886.5:n.367G>C
NM_007126.3:c.171G>C , LRG_657t1:c.171G>C NP_009057.1:p.Val57=
NM_001354927.1:c.36G>C NP_001341856.1:p.Val12=
NM_001354928.1:c.36G>C NP_001341857.1:p.Val12=
NM_007126.4:c.171G>C NP_009057.1:p.Val57=
NM_007126.5:c.171G>C MANE Select NP_009057.1:p.Val57=
NM_001354927.2:c.36G>C NP_001341856.1:p.Val12=
NM_001354928.2:c.36G>C NP_001341857.1:p.Val12=