Canonical Allele Identifier: CA1845849298

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068072A= , CM000671.2:g.35068072A=	GRCh38
NC_000009.11:g.35068069A= , CM000671.1:g.35068069A=	GRCh37
NC_000009.10:g.35058069A=	NCBI36
NG_007887.1:g.9671T= , LRG_657:g.9671T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.130-9T= MANE Select	ENSP00000351777.6:n.130-9T=
ENST00000417448.2:c.-6-9T=	ENSP00000399456.2:n.-6-9T=
ENST00000448530.6:c.-6-9T=	ENSP00000392088.2:n.-6-9T=
ENST00000480327.2:n.402-9T=
ENST00000676836.2:n.393-9T=
ENST00000677257.1:c.130-15T=	ENSP00000504354.1:n.130-15T=
ENST00000678018.1:c.*92T=	ENSP00000503811.1:n.*92T=
ENST00000678465.1:c.130-9T=	ENSP00000504259.1:n.130-9T=
ENST00000678650.1:c.-6-9T=	ENSP00000503426.1:n.-6-9T=
ENST00000679204.2:c.130-9T=	ENSP00000503131.2:n.130-9T=
ENST00000679449.1:c.140T=
ENST00000679599.1:n.400-9T=
ENST00000679647.1:c.130-9T=	ENSP00000506216.1:n.130-9T=
ENST00000679800.1:n.368-9T=
ENST00000679862.1:c.-6-9T=	ENSP00000504990.1:n.-6-9T=
ENST00000679902.1:c.130-9T=	ENSP00000506338.1:n.130-9T=
ENST00000680079.1:c.*51-9T=	ENSP00000506523.1:n.*51-9T=
ENST00000680900.1:c.125T=
ENST00000680916.1:c.130-9T=	ENSP00000505769.1:n.130-9T=
ENST00000681335.1:c.130-9T=	ENSP00000505230.1:n.130-9T=
ENST00000681386.1:c.-6-9T=	ENSP00000505509.1:n.-6-9T=
ENST00000681690.1:n.402-9T=
ENST00000681845.1:c.296-9T=
ENST00000358901.10:c.130-9T=	ENSP00000351777.6:n.130-9T=
ENST00000417448.1:c.-6-9T=	ENSP00000399456.1:n.-6-9T=
ENST00000448530.5:c.-6-9T=	ENSP00000392088.1:n.-6-9T=
ENST00000493886.5:n.326-9T=
NM_007126.3:c.130-9T= , LRG_657t1:c.130-9T=	NP_009057.1:n.130-9T=
NM_001354927.1:c.-6-9T=	NP_001341856.1:n.-6-9T=
NM_001354928.1:c.-6-9T=	NP_001341857.1:n.-6-9T=
NM_007126.4:c.130-9T=	NP_009057.1:n.130-9T=
NM_007126.5:c.130-9T= MANE Select	NP_009057.1:n.130-9T=
NM_001354927.2:c.-6-9T=	NP_001341856.1:n.-6-9T=
NM_001354928.2:c.-6-9T=	NP_001341857.1:n.-6-9T=