Canonical Allele Identifier: CA5039174

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35059634G>A , CM000671.2:g.35059634G>A	GRCh38
NC_000009.11:g.35059631G>A , CM000671.1:g.35059631G>A	GRCh37
NC_000009.10:g.35049631G>A	NCBI36
NG_007887.1:g.18109C>T , LRG_657:g.18109C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.1863C>T MANE Select	NP_009057.1:p.Gly621=
ENST00000358901.11:c.1863C>T MANE Select	ENSP00000351777.6:p.Gly621=
NM_001354927.1:c.1728C>T	NP_001341856.1:p.Gly576=
NM_001354927.2:c.1728C>T	NP_001341856.1:p.Gly576=
NM_001354928.1:c.1728C>T	NP_001341857.1:p.Gly576=
NM_001354928.2:c.1728C>T	NP_001341857.1:p.Gly576=
NM_007126.3:c.1863C>T , LRG_657t1:c.1863C>T	NP_009057.1:p.Gly621=
NM_007126.4:c.1863C>T	NP_009057.1:p.Gly621=
ENST00000358901.10:c.1863C>T	ENSP00000351777.6:p.Gly621=
ENST00000417448.2:c.1728C>T	ENSP00000399456.2:p.Gly576=
ENST00000448530.6:c.1728C>T	ENSP00000392088.2:p.Gly576=
ENST00000479300.1:n.259C>T
ENST00000479300.2:n.391C>T
ENST00000493886.5:n.2137C>T
ENST00000676836.2:n.2606C>T
ENST00000677257.1:c.1857C>T	ENSP00000504354.1:p.Gly619=
ENST00000678018.1:c.*1834C>T	ENSP00000503811.1:n.*1834C>T
ENST00000678465.1:c.*875C>T	ENSP00000504259.1:n.*875C>T
ENST00000678650.1:c.1728C>T	ENSP00000503426.1:p.Gly576=
ENST00000679204.2:c.*504C>T	ENSP00000503131.2:n.*504C>T
ENST00000679599.1:n.2919C>T
ENST00000679647.1:c.1863C>T	ENSP00000506216.1:p.Gly621=
ENST00000679800.1:n.2262C>T
ENST00000679862.1:c.1728C>T	ENSP00000504990.1:p.Gly576=
ENST00000679902.1:c.1863C>T	ENSP00000506338.1:p.Gly621=
ENST00000680916.1:c.1863C>T	ENSP00000505769.1:p.Gly621=
ENST00000681335.1:c.1863C>T	ENSP00000505230.1:p.Gly621=
ENST00000681690.1:n.2135C>T