Canonical Allele Identifier: CA373293725
Gene: VCP HGNC NCBI

Linked Data

gnomAD v4: 9-35067946-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35067946G>A , CM000671.2:g.35067946G>A GRCh38
NC_000009.11:g.35067943G>A , CM000671.1:g.35067943G>A GRCh37
NC_000009.10:g.35057943G>A NCBI36
NG_007887.1:g.9797C>T , LRG_657:g.9797C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358901.11:c.247C>T MANE Select ENSP00000351777.6:p.Arg83Trp
ENST00000417448.2:c.112C>T ENSP00000399456.2:p.Arg38Trp
ENST00000448530.6:c.112C>T ENSP00000392088.2:p.Arg38Trp
ENST00000480327.2:n.519C>T
ENST00000676836.2:n.510C>T
ENST00000677257.1:c.241C>T ENSP00000504354.1:p.Arg81Trp
ENST00000678018.1:c.*218C>T ENSP00000503811.1:n.*218C>T
ENST00000678465.1:c.247C>T ENSP00000504259.1:p.Arg83Trp
ENST00000678650.1:c.112C>T ENSP00000503426.1:p.Arg38Trp
ENST00000679204.2:c.247C>T ENSP00000503131.2:p.Arg83Trp
ENST00000679449.1:c.266C>T
ENST00000679599.1:n.517C>T
ENST00000679647.1:c.247C>T ENSP00000506216.1:p.Arg83Trp
ENST00000679800.1:n.485C>T
ENST00000679862.1:c.112C>T ENSP00000504990.1:p.Arg38Trp
ENST00000679902.1:c.247C>T ENSP00000506338.1:p.Arg83Trp
ENST00000680079.1:c.*168C>T ENSP00000506523.1:n.*168C>T
ENST00000680731.1:c.112C>T ENSP00000505497.1:p.Arg38Trp
ENST00000680900.1:c.251C>T
ENST00000680916.1:c.247C>T ENSP00000505769.1:p.Arg83Trp
ENST00000681335.1:c.247C>T ENSP00000505230.1:p.Arg83Trp
ENST00000681386.1:c.112C>T ENSP00000505509.1:p.Arg38Trp
ENST00000681690.1:n.519C>T
ENST00000681845.1:c.413C>T
ENST00000358901.10:c.247C>T ENSP00000351777.6:p.Arg83Trp
ENST00000417448.1:c.112C>T ENSP00000399456.1:p.Arg38Trp
ENST00000448530.5:c.112C>T ENSP00000392088.1:p.Arg38Trp
ENST00000493886.5:n.443C>T
NM_007126.3:c.247C>T , LRG_657t1:c.247C>T NP_009057.1:p.Arg83Trp
NM_001354927.1:c.112C>T NP_001341856.1:p.Arg38Trp
NM_001354928.1:c.112C>T NP_001341857.1:p.Arg38Trp
NM_007126.4:c.247C>T NP_009057.1:p.Arg83Trp
NM_007126.5:c.247C>T MANE Select NP_009057.1:p.Arg83Trp
NM_001354927.2:c.112C>T NP_001341856.1:p.Arg38Trp
NM_001354928.2:c.112C>T NP_001341857.1:p.Arg38Trp