Canonical Allele Identifier: CA464602374

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067935T>C , CM000671.2:g.35067935T>C	GRCh38
NC_000009.11:g.35067932T>C , CM000671.1:g.35067932T>C	GRCh37
NC_000009.10:g.35057932T>C	NCBI36
NG_007887.1:g.9808A>G , LRG_657:g.9808A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.258A>G MANE Select	NP_009057.1:p.Arg86=
ENST00000358901.11:c.258A>G MANE Select	ENSP00000351777.6:p.Arg86=
NM_001354927.1:c.123A>G	NP_001341856.1:p.Arg41=
NM_001354927.2:c.123A>G	NP_001341856.1:p.Arg41=
NM_001354928.1:c.123A>G	NP_001341857.1:p.Arg41=
NM_001354928.2:c.123A>G	NP_001341857.1:p.Arg41=
NM_007126.3:c.258A>G , LRG_657t1:c.258A>G	NP_009057.1:p.Arg86=
NM_007126.4:c.258A>G	NP_009057.1:p.Arg86=
ENST00000358901.10:c.258A>G	ENSP00000351777.6:p.Arg86=
ENST00000417448.1:c.123A>G	ENSP00000399456.1:p.Arg41=
ENST00000417448.2:c.123A>G	ENSP00000399456.2:p.Arg41=
ENST00000448530.5:c.123A>G	ENSP00000392088.1:p.Arg41=
ENST00000448530.6:c.123A>G	ENSP00000392088.2:p.Arg41=
ENST00000480327.2:n.530A>G
ENST00000493886.5:n.454A>G
ENST00000676836.2:n.521A>G
ENST00000677257.1:c.252A>G	ENSP00000504354.1:p.Arg84=
ENST00000678018.1:c.*229A>G	ENSP00000503811.1:n.*229A>G
ENST00000678465.1:c.258A>G	ENSP00000504259.1:p.Arg86=
ENST00000678650.1:c.123A>G	ENSP00000503426.1:p.Arg41=
ENST00000679204.2:c.258A>G	ENSP00000503131.2:p.Arg86=
ENST00000679449.1:c.277A>G
ENST00000679599.1:n.528A>G
ENST00000679647.1:c.258A>G	ENSP00000506216.1:p.Arg86=
ENST00000679800.1:n.496A>G
ENST00000679862.1:c.123A>G	ENSP00000504990.1:p.Arg41=
ENST00000679902.1:c.258A>G	ENSP00000506338.1:p.Arg86=
ENST00000680079.1:c.*179A>G	ENSP00000506523.1:n.*179A>G
ENST00000680731.1:c.123A>G	ENSP00000505497.1:p.Arg41=
ENST00000680900.1:c.262A>G
ENST00000680916.1:c.258A>G	ENSP00000505769.1:p.Arg86=
ENST00000681335.1:c.258A>G	ENSP00000505230.1:p.Arg86=
ENST00000681386.1:c.123A>G	ENSP00000505509.1:p.Arg41=
ENST00000681690.1:n.530A>G
ENST00000681845.1:c.424A>G