Canonical Allele Identifier: CA10629987

Gene: VCP

Linked Data

• ClinVar Variation Id: 366713
• ClinVar RCV Id: RCV000260516 ; RCV000373981
• dbSNP Id: rs886063890
• gnomAD v2: 9-35056942-G-C
• gnomAD v3: 9-35056945-G-C
• gnomAD v4: 9-35056945-G-C
• MyVariant Identifiers: chr9:g.35056942G>C (hg19) ; chr9:g.35056945G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35056945G>C , CM000671.2:g.35056945G>C	GRCh38
NC_000009.11:g.35056942G>C , CM000671.1:g.35056942G>C	GRCh37
NC_000009.10:g.35046942G>C	NCBI36
NG_007887.1:g.20798C>G , LRG_657:g.20798C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.*172C>G MANE Select	ENSP00000351777.6:n.*172C>G
ENST00000417448.2:c.*172C>G	ENSP00000399456.2:n.*172C>G
ENST00000448530.6:c.*172C>G	ENSP00000392088.2:n.*172C>G
ENST00000479300.2:n.1121C>G
ENST00000676836.2:n.3336C>G
ENST00000677257.1:c.*172C>G	ENSP00000504354.1:n.*172C>G
ENST00000678018.1:c.*2564C>G	ENSP00000503811.1:n.*2564C>G
ENST00000678465.1:c.*1605C>G	ENSP00000504259.1:n.*1605C>G
ENST00000678650.1:c.*172C>G	ENSP00000503426.1:n.*172C>G
ENST00000679204.2:c.*1234C>G	ENSP00000503131.2:n.*1234C>G
ENST00000679599.1:n.5182C>G
ENST00000679647.1:c.*32C>G	ENSP00000506216.1:n.*32C>G
ENST00000679800.1:n.2992C>G
ENST00000679862.1:c.*172C>G	ENSP00000504990.1:n.*172C>G
ENST00000679902.1:c.*427C>G	ENSP00000506338.1:n.*427C>G
ENST00000680916.1:c.*558C>G	ENSP00000505769.1:n.*558C>G
ENST00000681335.1:c.*172C>G	ENSP00000505230.1:n.*172C>G
ENST00000681537.1:c.422C>G	ENSP00000505847.1:n.422C>G
ENST00000681690.1:n.4398C>G
ENST00000358901.10:c.*172C>G	ENSP00000351777.6:n.*172C>G
ENST00000493886.5:n.2867C>G
NM_007126.3:c.*172C>G , LRG_657t1:c.*172C>G	NP_009057.1:n.*172C>G
NM_001354927.1:c.*172C>G	NP_001341856.1:n.*172C>G
NM_001354928.1:c.*172C>G	NP_001341857.1:n.*172C>G
NM_007126.4:c.*172C>G	NP_009057.1:n.*172C>G
NM_007126.5:c.*172C>G MANE Select	NP_009057.1:n.*172C>G
NM_001354927.2:c.*172C>G	NP_001341856.1:n.*172C>G
NM_001354928.2:c.*172C>G	NP_001341857.1:n.*172C>G