Canonical Allele Identifier: CA1845848970

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067903C= , CM000671.2:g.35067903C=	GRCh38
NC_000009.11:g.35067900C= , CM000671.1:g.35067900C=	GRCh37
NC_000009.10:g.35057900C=	NCBI36
NG_007887.1:g.9840G= , LRG_657:g.9840G=

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.290G= MANE Select	NP_009057.1:p.Gly97=
ENST00000358901.11:c.290G= MANE Select	ENSP00000351777.6:p.Gly97=
NM_001354927.1:c.155G=	NP_001341856.1:p.Gly52=
NM_001354927.2:c.155G=	NP_001341856.1:p.Gly52=
NM_001354928.1:c.155G=	NP_001341857.1:p.Gly52=
NM_001354928.2:c.155G=	NP_001341857.1:p.Gly52=
NM_007126.3:c.290G= , LRG_657t1:c.290G=	NP_009057.1:p.Gly97=
NM_007126.4:c.290G=	NP_009057.1:p.Gly97=
ENST00000358901.10:c.290G=	ENSP00000351777.6:p.Gly97=
ENST00000417448.1:c.155G=	ENSP00000399456.1:p.Gly52=
ENST00000417448.2:c.155G=	ENSP00000399456.2:p.Gly52=
ENST00000448530.5:c.155G=	ENSP00000392088.1:p.Gly52=
ENST00000448530.6:c.155G=	ENSP00000392088.2:p.Gly52=
ENST00000480327.2:n.562G=
ENST00000493886.5:n.486G=
ENST00000676836.2:n.553G=
ENST00000677257.1:c.284G=	ENSP00000504354.1:p.Gly95=
ENST00000678018.1:c.*261G=	ENSP00000503811.1:n.*261G=
ENST00000678465.1:c.290G=	ENSP00000504259.1:p.Gly97=
ENST00000678650.1:c.155G=	ENSP00000503426.1:p.Gly52=
ENST00000679204.2:c.290G=	ENSP00000503131.2:p.Gly97=
ENST00000679449.1:c.309G=
ENST00000679599.1:n.560G=
ENST00000679647.1:c.290G=	ENSP00000506216.1:p.Gly97=
ENST00000679800.1:n.528G=
ENST00000679862.1:c.155G=	ENSP00000504990.1:p.Gly52=
ENST00000679902.1:c.290G=	ENSP00000506338.1:p.Gly97=
ENST00000680079.1:c.*211G=	ENSP00000506523.1:n.*211G=
ENST00000680731.1:c.155G=	ENSP00000505497.1:p.Gly52=
ENST00000680900.1:c.294G=
ENST00000680916.1:c.290G=	ENSP00000505769.1:p.Gly97=
ENST00000681335.1:c.290G=	ENSP00000505230.1:p.Gly97=
ENST00000681386.1:c.155G=	ENSP00000505509.1:p.Gly52=
ENST00000681690.1:n.562G=
ENST00000681845.1:c.456G=