Canonical Allele Identifier: CA464602541

Gene: VCP

Linked Data

• gnomAD v4: 9-35068052-A-G
• MyVariant Identifiers: chr9:g.35068049A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068052A>G , CM000671.2:g.35068052A>G	GRCh38
NC_000009.11:g.35068049A>G , CM000671.1:g.35068049A>G	GRCh37
NC_000009.10:g.35058049A>G	NCBI36
NG_007887.1:g.9691T>C , LRG_657:g.9691T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.141T>C MANE Select	ENSP00000351777.6:p.Asp47=
ENST00000417448.2:c.6T>C	ENSP00000399456.2:p.Asp2=
ENST00000448530.6:c.6T>C	ENSP00000392088.2:p.Asp2=
ENST00000480327.2:n.413T>C
ENST00000676836.2:n.404T>C
ENST00000677257.1:c.135T>C	ENSP00000504354.1:p.Asp45=
ENST00000678018.1:c.*112T>C	ENSP00000503811.1:n.*112T>C
ENST00000678465.1:c.141T>C	ENSP00000504259.1:p.Asp47=
ENST00000678650.1:c.6T>C	ENSP00000503426.1:p.Asp2=
ENST00000679204.2:c.141T>C	ENSP00000503131.2:p.Asp47=
ENST00000679449.1:c.160T>C
ENST00000679599.1:n.411T>C
ENST00000679647.1:c.141T>C	ENSP00000506216.1:p.Asp47=
ENST00000679800.1:n.379T>C
ENST00000679862.1:c.6T>C	ENSP00000504990.1:p.Asp2=
ENST00000679902.1:c.141T>C	ENSP00000506338.1:p.Asp47=
ENST00000680079.1:c.*62T>C	ENSP00000506523.1:n.*62T>C
ENST00000680731.1:c.6T>C	ENSP00000505497.1:p.Asp2=
ENST00000680900.1:c.145T>C
ENST00000680916.1:c.141T>C	ENSP00000505769.1:p.Asp47=
ENST00000681335.1:c.141T>C	ENSP00000505230.1:p.Asp47=
ENST00000681386.1:c.6T>C	ENSP00000505509.1:p.Asp2=
ENST00000681690.1:n.413T>C
ENST00000681845.1:c.307T>C
ENST00000358901.10:c.141T>C	ENSP00000351777.6:p.Asp47=
ENST00000417448.1:c.6T>C	ENSP00000399456.1:p.Asp2=
ENST00000448530.5:c.6T>C	ENSP00000392088.1:p.Asp2=
ENST00000493886.5:n.337T>C
NM_007126.3:c.141T>C , LRG_657t1:c.141T>C	NP_009057.1:p.Asp47=
NM_001354927.1:c.6T>C	NP_001341856.1:p.Asp2=
NM_001354928.1:c.6T>C	NP_001341857.1:p.Asp2=
NM_007126.4:c.141T>C	NP_009057.1:p.Asp47=
NM_007126.5:c.141T>C MANE Select	NP_009057.1:p.Asp47=
NM_001354927.2:c.6T>C	NP_001341856.1:p.Asp2=
NM_001354928.2:c.6T>C	NP_001341857.1:p.Asp2=