Canonical Allele Identifier: CA1845848734

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067821A= , CM000671.2:g.35067821A=	GRCh38
NC_000009.11:g.35067818A= , CM000671.1:g.35067818A=	GRCh37
NC_000009.10:g.35057818A=	NCBI36
NG_007887.1:g.9922T= , LRG_657:g.9922T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.302+70T= MANE Select	ENSP00000351777.6:n.302+70T=
ENST00000417448.2:c.167+70T=	ENSP00000399456.2:n.167+70T=
ENST00000448530.6:c.167+70T=	ENSP00000392088.2:n.167+70T=
ENST00000480327.2:n.574+70T=
ENST00000676836.2:n.565+70T=
ENST00000677257.1:c.296+70T=	ENSP00000504354.1:n.296+70T=
ENST00000678018.1:c.*273+70T=	ENSP00000503811.1:n.*273+70T=
ENST00000678465.1:c.302+70T=	ENSP00000504259.1:n.302+70T=
ENST00000678650.1:c.167+70T=	ENSP00000503426.1:n.167+70T=
ENST00000679204.2:c.302+70T=	ENSP00000503131.2:n.302+70T=
ENST00000679599.1:n.572+70T=
ENST00000679647.1:c.302+70T=	ENSP00000506216.1:n.302+70T=
ENST00000679800.1:n.540+70T=
ENST00000679862.1:c.167+70T=	ENSP00000504990.1:n.167+70T=
ENST00000679902.1:c.302+70T=	ENSP00000506338.1:n.302+70T=
ENST00000680079.1:c.*223+70T=	ENSP00000506523.1:n.*223+70T=
ENST00000680731.1:c.167+70T=	ENSP00000505497.1:n.167+70T=
ENST00000680916.1:c.302+70T=	ENSP00000505769.1:n.302+70T=
ENST00000681335.1:c.302+70T=	ENSP00000505230.1:n.302+70T=
ENST00000681690.1:n.574+70T=
ENST00000681845.1:c.468+70T=
ENST00000358901.10:c.302+70T=	ENSP00000351777.6:n.302+70T=
ENST00000417448.1:c.167+70T=	ENSP00000399456.1:n.167+70T=
ENST00000448530.5:c.167+70T=	ENSP00000392088.1:n.167+70T=
ENST00000493886.5:n.498+70T=
NM_007126.3:c.302+70T= , LRG_657t1:c.302+70T=	NP_009057.1:n.302+70T=
NM_001354927.1:c.167+70T=	NP_001341856.1:n.167+70T=
NM_001354928.1:c.167+70T=	NP_001341857.1:n.167+70T=
NM_007126.4:c.302+70T=	NP_009057.1:n.302+70T=
NM_007126.5:c.302+70T= MANE Select	NP_009057.1:n.302+70T=
NM_001354927.2:c.167+70T=	NP_001341856.1:n.167+70T=
NM_001354928.2:c.167+70T=	NP_001341857.1:n.167+70T=