Canonical Allele Identifier: CA373276470

Gene: VCP

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35059723C>G , CM000671.2:g.35059723C>G	GRCh38
NC_000009.11:g.35059720C>G , CM000671.1:g.35059720C>G	GRCh37
NC_000009.10:g.35049720C>G	NCBI36
NG_007887.1:g.18020G>C , LRG_657:g.18020G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.1774G>C MANE Select	ENSP00000351777.6:p.Asp592His
ENST00000417448.2:c.1639G>C	ENSP00000399456.2:p.Asp547His
ENST00000448530.6:c.1639G>C	ENSP00000392088.2:p.Asp547His
ENST00000479300.2:n.302G>C
ENST00000676836.2:n.2517G>C
ENST00000677257.1:c.1768G>C	ENSP00000504354.1:p.Asp590His
ENST00000678018.1:c.*1745G>C	ENSP00000503811.1:n.*1745G>C
ENST00000678465.1:c.*786G>C	ENSP00000504259.1:n.*786G>C
ENST00000678650.1:c.1639G>C	ENSP00000503426.1:p.Asp547His
ENST00000679204.2:c.*415G>C	ENSP00000503131.2:n.*415G>C
ENST00000679599.1:n.2830G>C
ENST00000679647.1:c.1774G>C	ENSP00000506216.1:p.Asp592His
ENST00000679800.1:n.2173G>C
ENST00000679862.1:c.1639G>C	ENSP00000504990.1:p.Asp547His
ENST00000679902.1:c.1774G>C	ENSP00000506338.1:p.Asp592His
ENST00000680916.1:c.1774G>C	ENSP00000505769.1:p.Asp592His
ENST00000681335.1:c.1774G>C	ENSP00000505230.1:p.Asp592His
ENST00000681690.1:n.2046G>C
ENST00000358901.10:c.1774G>C	ENSP00000351777.6:p.Asp592His
ENST00000479300.1:n.170G>C
ENST00000493886.5:n.2048G>C
NM_007126.3:c.1774G>C , LRG_657t1:c.1774G>C	NP_009057.1:p.Asp592His
NM_001354927.1:c.1639G>C	NP_001341856.1:p.Asp547His
NM_001354928.1:c.1639G>C	NP_001341857.1:p.Asp547His
NM_007126.4:c.1774G>C	NP_009057.1:p.Asp592His
NM_007126.5:c.1774G>C MANE Select	NP_009057.1:p.Asp592His
NM_001354927.2:c.1639G>C	NP_001341856.1:p.Asp547His
NM_001354928.2:c.1639G>C	NP_001341857.1:p.Asp547His