Canonical Allele Identifier: CA373289512

Gene: VCP

Linked Data

• ClinVar Variation Id: 532761
• ClinVar RCV Id: RCV000639654 ; RCV000993545 ; RCV001535609
• dbSNP Id: rs1554668805
• MyVariant Identifiers: chr9:g.35065346C>G (hg19) ; chr9:g.35065349C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35065349C>G , CM000671.2:g.35065349C>G	GRCh38
NC_000009.11:g.35065346C>G , CM000671.1:g.35065346C>G	GRCh37
NC_000009.10:g.35055346C>G	NCBI36
NG_007887.1:g.12394G>C , LRG_657:g.12394G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.478G>C MANE Select	ENSP00000351777.6:p.Ala160Pro
ENST00000417448.2:c.343G>C	ENSP00000399456.2:p.Ala115Pro
ENST00000448530.6:c.343G>C	ENSP00000392088.2:p.Ala115Pro
ENST00000480327.2:n.750G>C
ENST00000676836.2:n.824G>C
ENST00000677257.1:c.472G>C	ENSP00000504354.1:p.Ala158Pro
ENST00000678018.1:c.*449G>C	ENSP00000503811.1:n.*449G>C
ENST00000678465.1:c.478G>C	ENSP00000504259.1:p.Ala160Pro
ENST00000678650.1:c.343G>C	ENSP00000503426.1:p.Ala115Pro
ENST00000679204.2:c.478G>C	ENSP00000503131.2:p.Ala160Pro
ENST00000679599.1:n.748G>C
ENST00000679647.1:c.478G>C	ENSP00000506216.1:p.Ala160Pro
ENST00000679800.1:n.799G>C
ENST00000679862.1:c.343G>C	ENSP00000504990.1:p.Ala115Pro
ENST00000679902.1:c.478G>C	ENSP00000506338.1:p.Ala160Pro
ENST00000680520.1:c.33G>C
ENST00000680731.1:c.200G>C	ENSP00000505497.1:p.Cys67Ser
ENST00000680916.1:c.478G>C	ENSP00000505769.1:p.Ala160Pro
ENST00000681335.1:c.478G>C	ENSP00000505230.1:p.Ala160Pro
ENST00000681562.1:c.230G>C
ENST00000681690.1:n.750G>C
ENST00000681789.1:c.33G>C
ENST00000681845.1:c.644G>C
ENST00000358901.10:c.478G>C	ENSP00000351777.6:p.Ala160Pro
ENST00000417448.1:c.343G>C	ENSP00000399456.1:p.Ala115Pro
ENST00000448530.5:c.343G>C	ENSP00000392088.1:p.Ala115Pro
ENST00000493886.5:n.674G>C
NM_007126.3:c.478G>C , LRG_657t1:c.478G>C	NP_009057.1:p.Ala160Pro
NM_001354927.1:c.343G>C	NP_001341856.1:p.Ala115Pro
NM_001354928.1:c.343G>C	NP_001341857.1:p.Ala115Pro
NM_007126.4:c.478G>C	NP_009057.1:p.Ala160Pro
NM_007126.5:c.478G>C MANE Select	NP_009057.1:p.Ala160Pro
NM_001354927.2:c.343G>C	NP_001341856.1:p.Ala115Pro
NM_001354928.2:c.343G>C	NP_001341857.1:p.Ala115Pro