Canonical Allele Identifier: CA464601983

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35059568G>A , CM000671.2:g.35059568G>A	GRCh38
NC_000009.11:g.35059565G>A , CM000671.1:g.35059565G>A	GRCh37
NC_000009.10:g.35049565G>A	NCBI36
NG_007887.1:g.18175C>T , LRG_657:g.18175C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.1929C>T MANE Select	NP_009057.1:p.Ile643=
ENST00000358901.11:c.1929C>T MANE Select	ENSP00000351777.6:p.Ile643=
NM_001354927.1:c.1794C>T	NP_001341856.1:p.Ile598=
NM_001354927.2:c.1794C>T	NP_001341856.1:p.Ile598=
NM_001354928.1:c.1794C>T	NP_001341857.1:p.Ile598=
NM_001354928.2:c.1794C>T	NP_001341857.1:p.Ile598=
NM_007126.3:c.1929C>T , LRG_657t1:c.1929C>T	NP_009057.1:p.Ile643=
NM_007126.4:c.1929C>T	NP_009057.1:p.Ile643=
ENST00000358901.10:c.1929C>T	ENSP00000351777.6:p.Ile643=
ENST00000417448.2:c.1794C>T	ENSP00000399456.2:p.Ile598=
ENST00000448530.6:c.1794C>T	ENSP00000392088.2:p.Ile598=
ENST00000479300.1:n.325C>T
ENST00000479300.2:n.457C>T
ENST00000493886.5:n.2203C>T
ENST00000676836.2:n.2672C>T
ENST00000677257.1:c.1923C>T	ENSP00000504354.1:p.Ile641=
ENST00000678018.1:c.*1900C>T	ENSP00000503811.1:n.*1900C>T
ENST00000678465.1:c.*941C>T	ENSP00000504259.1:n.*941C>T
ENST00000678650.1:c.1794C>T	ENSP00000503426.1:p.Ile598=
ENST00000679204.2:c.*570C>T	ENSP00000503131.2:n.*570C>T
ENST00000679599.1:n.2985C>T
ENST00000679647.1:c.1929C>T	ENSP00000506216.1:p.Ile643=
ENST00000679800.1:n.2328C>T
ENST00000679862.1:c.1794C>T	ENSP00000504990.1:p.Ile598=
ENST00000679902.1:c.1929C>T	ENSP00000506338.1:p.Ile643=
ENST00000680916.1:c.1929C>T	ENSP00000505769.1:p.Ile643=
ENST00000681335.1:c.1929C>T	ENSP00000505230.1:p.Ile643=
ENST00000681690.1:n.2201C>T