Canonical Allele Identifier: CA464602311

Gene: VCP

Linked Data

• MyVariant Identifiers: chr9:g.35067911A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067914A>G , CM000671.2:g.35067914A>G	GRCh38
NC_000009.11:g.35067911A>G , CM000671.1:g.35067911A>G	GRCh37
NC_000009.10:g.35057911A>G	NCBI36
NG_007887.1:g.9829T>C , LRG_657:g.9829T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.279T>C MANE Select	ENSP00000351777.6:p.Arg93=
ENST00000417448.2:c.144T>C	ENSP00000399456.2:p.Arg48=
ENST00000448530.6:c.144T>C	ENSP00000392088.2:p.Arg48=
ENST00000480327.2:n.551T>C
ENST00000676836.2:n.542T>C
ENST00000677257.1:c.273T>C	ENSP00000504354.1:p.Arg91=
ENST00000678018.1:c.*250T>C	ENSP00000503811.1:n.*250T>C
ENST00000678465.1:c.279T>C	ENSP00000504259.1:p.Arg93=
ENST00000678650.1:c.144T>C	ENSP00000503426.1:p.Arg48=
ENST00000679204.2:c.279T>C	ENSP00000503131.2:p.Arg93=
ENST00000679449.1:c.298T>C
ENST00000679599.1:n.549T>C
ENST00000679647.1:c.279T>C	ENSP00000506216.1:p.Arg93=
ENST00000679800.1:n.517T>C
ENST00000679862.1:c.144T>C	ENSP00000504990.1:p.Arg48=
ENST00000679902.1:c.279T>C	ENSP00000506338.1:p.Arg93=
ENST00000680079.1:c.*200T>C	ENSP00000506523.1:n.*200T>C
ENST00000680731.1:c.144T>C	ENSP00000505497.1:p.Arg48=
ENST00000680900.1:c.283T>C
ENST00000680916.1:c.279T>C	ENSP00000505769.1:p.Arg93=
ENST00000681335.1:c.279T>C	ENSP00000505230.1:p.Arg93=
ENST00000681386.1:c.144T>C	ENSP00000505509.1:p.Arg48=
ENST00000681690.1:n.551T>C
ENST00000681845.1:c.445T>C
ENST00000358901.10:c.279T>C	ENSP00000351777.6:p.Arg93=
ENST00000417448.1:c.144T>C	ENSP00000399456.1:p.Arg48=
ENST00000448530.5:c.144T>C	ENSP00000392088.1:p.Arg48=
ENST00000493886.5:n.475T>C
NM_007126.3:c.279T>C , LRG_657t1:c.279T>C	NP_009057.1:p.Arg93=
NM_001354927.1:c.144T>C	NP_001341856.1:p.Arg48=
NM_001354928.1:c.144T>C	NP_001341857.1:p.Arg48=
NM_007126.4:c.279T>C	NP_009057.1:p.Arg93=
NM_007126.5:c.279T>C MANE Select	NP_009057.1:p.Arg93=
NM_001354927.2:c.144T>C	NP_001341856.1:p.Arg48=
NM_001354928.2:c.144T>C	NP_001341857.1:p.Arg48=