Canonical Allele Identifier: CA1845849356

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068104C= , CM000671.2:g.35068104C=	GRCh38
NC_000009.11:g.35068101C= , CM000671.1:g.35068101C=	GRCh37
NC_000009.10:g.35058101C=	NCBI36
NG_007887.1:g.9639G= , LRG_657:g.9639G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.130-41G= MANE Select	ENSP00000351777.6:n.130-41G=
ENST00000417448.2:c.-6-41G=	ENSP00000399456.2:n.-6-41G=
ENST00000448530.6:c.-6-41G=	ENSP00000392088.2:n.-6-41G=
ENST00000480327.2:n.402-41G=
ENST00000676836.2:n.393-41G=
ENST00000677257.1:c.130-47G=	ENSP00000504354.1:n.130-47G=
ENST00000678018.1:c.*60G=	ENSP00000503811.1:n.*60G=
ENST00000678465.1:c.130-41G=	ENSP00000504259.1:n.130-41G=
ENST00000678650.1:c.-6-41G=	ENSP00000503426.1:n.-6-41G=
ENST00000679204.2:c.130-41G=	ENSP00000503131.2:n.130-41G=
ENST00000679449.1:c.113-5G=
ENST00000679599.1:n.400-41G=
ENST00000679647.1:c.130-41G=	ENSP00000506216.1:n.130-41G=
ENST00000679800.1:n.368-41G=
ENST00000679862.1:c.-6-41G=	ENSP00000504990.1:n.-6-41G=
ENST00000679902.1:c.130-41G=	ENSP00000506338.1:n.130-41G=
ENST00000680079.1:c.*51-41G=	ENSP00000506523.1:n.*51-41G=
ENST00000680900.1:c.113-20G=
ENST00000680916.1:c.130-41G=	ENSP00000505769.1:n.130-41G=
ENST00000681335.1:c.130-41G=	ENSP00000505230.1:n.130-41G=
ENST00000681386.1:c.-6-41G=	ENSP00000505509.1:n.-6-41G=
ENST00000681690.1:n.402-41G=
ENST00000681845.1:c.296-41G=
ENST00000358901.10:c.130-41G=	ENSP00000351777.6:n.130-41G=
ENST00000417448.1:c.-6-41G=	ENSP00000399456.1:n.-6-41G=
ENST00000448530.5:c.-6-41G=	ENSP00000392088.1:n.-6-41G=
ENST00000493886.5:n.326-41G=
NM_007126.3:c.130-41G= , LRG_657t1:c.130-41G=	NP_009057.1:n.130-41G=
NM_001354927.1:c.-6-41G=	NP_001341856.1:n.-6-41G=
NM_001354928.1:c.-6-41G=	NP_001341857.1:n.-6-41G=
NM_007126.4:c.130-41G=	NP_009057.1:n.130-41G=
NM_007126.5:c.130-41G= MANE Select	NP_009057.1:n.130-41G=
NM_001354927.2:c.-6-41G=	NP_001341856.1:n.-6-41G=
NM_001354928.2:c.-6-41G=	NP_001341857.1:n.-6-41G=