Canonical Allele Identifier: CA1845842264

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35065274C= , CM000671.2:g.35065274C=	GRCh38
NC_000009.11:g.35065271C= , CM000671.1:g.35065271C=	GRCh37
NC_000009.10:g.35055271C=	NCBI36
NG_007887.1:g.12469G= , LRG_657:g.12469G=

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.553G= MANE Select	NP_009057.1:p.Glu185=
ENST00000358901.11:c.553G= MANE Select	ENSP00000351777.6:p.Glu185=
NM_001354927.1:c.418G=	NP_001341856.1:p.Glu140=
NM_001354927.2:c.418G=	NP_001341856.1:p.Glu140=
NM_001354928.1:c.418G=	NP_001341857.1:p.Glu140=
NM_001354928.2:c.418G=	NP_001341857.1:p.Glu140=
NM_007126.3:c.553G= , LRG_657t1:c.553G=	NP_009057.1:p.Glu185=
NM_007126.4:c.553G=	NP_009057.1:p.Glu185=
ENST00000358901.10:c.553G=	ENSP00000351777.6:p.Glu185=
ENST00000417448.2:c.418G=	ENSP00000399456.2:p.Glu140=
ENST00000448530.5:c.418G=	ENSP00000392088.1:p.Glu140=
ENST00000448530.6:c.418G=	ENSP00000392088.2:p.Glu140=
ENST00000480327.2:n.825G=
ENST00000493886.5:n.749G=
ENST00000676836.2:n.899G=
ENST00000677257.1:c.547G=	ENSP00000504354.1:p.Glu183=
ENST00000678018.1:c.*524G=	ENSP00000503811.1:n.*524G=
ENST00000678465.1:c.553G=	ENSP00000504259.1:p.Glu185=
ENST00000678650.1:c.418G=	ENSP00000503426.1:p.Glu140=
ENST00000679204.2:c.553G=	ENSP00000503131.2:p.Glu185=
ENST00000679599.1:n.823G=
ENST00000679647.1:c.553G=	ENSP00000506216.1:p.Glu185=
ENST00000679800.1:n.874G=
ENST00000679862.1:c.418G=	ENSP00000504990.1:p.Glu140=
ENST00000679902.1:c.553G=	ENSP00000506338.1:p.Glu185=
ENST00000680520.1:c.108G=
ENST00000680731.1:c.*41G=	ENSP00000505497.1:n.*41G=
ENST00000680834.1:c.35G=
ENST00000680916.1:c.553G=	ENSP00000505769.1:p.Glu185=
ENST00000681335.1:c.553G=	ENSP00000505230.1:p.Glu185=
ENST00000681562.1:c.305G=
ENST00000681690.1:n.825G=
ENST00000681789.1:c.108G=