Canonical Allele Identifier: CA10627278

Gene: VCP

Linked Data

• ClinVar Variation Id: 366712
• ClinVar RCV Id: RCV000275373 ; RCV000319333
• dbSNP Id: rs886063889
• gnomAD v3: 9-35056933-C-T
• gnomAD v4: 9-35056933-C-T
• MyVariant Identifiers: chr9:g.35056930C>T (hg19) ; chr9:g.35056933C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35056933C>T , CM000671.2:g.35056933C>T	GRCh38
NC_000009.11:g.35056930C>T , CM000671.1:g.35056930C>T	GRCh37
NC_000009.10:g.35046930C>T	NCBI36
NG_007887.1:g.20810G>A , LRG_657:g.20810G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.*184G>A MANE Select	ENSP00000351777.6:n.*184G>A
ENST00000417448.2:c.*184G>A	ENSP00000399456.2:n.*184G>A
ENST00000448530.6:c.*184G>A	ENSP00000392088.2:n.*184G>A
ENST00000479300.2:n.1133G>A
ENST00000676836.2:n.3348G>A
ENST00000677257.1:c.*184G>A	ENSP00000504354.1:n.*184G>A
ENST00000678018.1:c.*2576G>A	ENSP00000503811.1:n.*2576G>A
ENST00000678465.1:c.*1617G>A	ENSP00000504259.1:n.*1617G>A
ENST00000678650.1:c.*184G>A	ENSP00000503426.1:n.*184G>A
ENST00000679204.2:c.*1246G>A	ENSP00000503131.2:n.*1246G>A
ENST00000679599.1:n.5194G>A
ENST00000679647.1:c.*44G>A	ENSP00000506216.1:n.*44G>A
ENST00000679800.1:n.3004G>A
ENST00000679862.1:c.*184G>A	ENSP00000504990.1:n.*184G>A
ENST00000679902.1:c.*439G>A	ENSP00000506338.1:n.*439G>A
ENST00000680916.1:c.*570G>A	ENSP00000505769.1:n.*570G>A
ENST00000681335.1:c.*184G>A	ENSP00000505230.1:n.*184G>A
ENST00000681537.1:c.434G>A	ENSP00000505847.1:n.434G>A
ENST00000681690.1:n.4410G>A
ENST00000358901.10:c.*184G>A	ENSP00000351777.6:n.*184G>A
ENST00000493886.5:n.2879G>A
NM_007126.3:c.*184G>A , LRG_657t1:c.*184G>A	NP_009057.1:n.*184G>A
NM_001354927.1:c.*184G>A	NP_001341856.1:n.*184G>A
NM_001354928.1:c.*184G>A	NP_001341857.1:n.*184G>A
NM_007126.4:c.*184G>A	NP_009057.1:n.*184G>A
NM_007126.5:c.*184G>A MANE Select	NP_009057.1:n.*184G>A
NM_001354927.2:c.*184G>A	NP_001341856.1:n.*184G>A
NM_001354928.2:c.*184G>A	NP_001341857.1:n.*184G>A