Canonical Allele Identifier: CA5039250

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35060823C>T , CM000671.2:g.35060823C>T	GRCh38
NC_000009.11:g.35060820C>T , CM000671.1:g.35060820C>T	GRCh37
NC_000009.10:g.35050820C>T	NCBI36
NG_007887.1:g.16920G>A , LRG_657:g.16920G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.1460G>A MANE Select	NP_009057.1:p.Arg487His
ENST00000358901.11:c.1460G>A MANE Select	ENSP00000351777.6:p.Arg487His
NM_001354927.1:c.1325G>A	NP_001341856.1:p.Arg442His
NM_001354927.2:c.1325G>A	NP_001341856.1:p.Arg442His
NM_001354928.1:c.1325G>A	NP_001341857.1:p.Arg442His
NM_001354928.2:c.1325G>A	NP_001341857.1:p.Arg442His
NM_007126.3:c.1460G>A , LRG_657t1:c.1460G>A	NP_009057.1:p.Arg487His
NM_007126.4:c.1460G>A	NP_009057.1:p.Arg487His
ENST00000358901.10:c.1460G>A	ENSP00000351777.6:p.Arg487His
ENST00000417448.2:c.1325G>A	ENSP00000399456.2:p.Arg442His
ENST00000448530.6:c.1325G>A	ENSP00000392088.2:p.Arg442His
ENST00000480327.1:n.320G>A
ENST00000480327.2:n.1598G>A
ENST00000493886.5:n.1734G>A
ENST00000676836.2:n.2203G>A
ENST00000677257.1:c.1454G>A	ENSP00000504354.1:p.Arg485His
ENST00000678018.1:c.*1431G>A	ENSP00000503811.1:n.*1431G>A
ENST00000678465.1:c.*472G>A	ENSP00000504259.1:n.*472G>A
ENST00000678650.1:c.1325G>A	ENSP00000503426.1:p.Arg442His
ENST00000679204.2:c.*101G>A	ENSP00000503131.2:n.*101G>A
ENST00000679599.1:n.1730G>A
ENST00000679647.1:c.1460G>A	ENSP00000506216.1:p.Arg487His
ENST00000679800.1:n.1859G>A
ENST00000679862.1:c.1325G>A	ENSP00000504990.1:p.Arg442His
ENST00000679902.1:c.1460G>A	ENSP00000506338.1:p.Arg487His
ENST00000680916.1:c.1460G>A	ENSP00000505769.1:p.Arg487His
ENST00000681335.1:c.1460G>A	ENSP00000505230.1:p.Arg487His
ENST00000681690.1:n.1732G>A