Canonical Allele Identifier: CA10633600

Gene: VCP

Linked Data

• ClinVar Variation Id: 366706
• ClinVar RCV Id: RCV000279189 ; RCV000373728 ; RCV003430970
• dbSNP Id: rs537730311
• gnomAD v2: 9-35056414-G-T
• gnomAD v3: 9-35056417-G-T
• gnomAD v4: 9-35056417-G-T
• MyVariant Identifiers: chr9:g.35056414G>T (hg19) ; chr9:g.35056417G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35056417G>T , CM000671.2:g.35056417G>T	GRCh38
NC_000009.11:g.35056414G>T , CM000671.1:g.35056414G>T	GRCh37
NC_000009.10:g.35046414G>T	NCBI36
NG_007887.1:g.21326C>A , LRG_657:g.21326C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.*700C>A MANE Select	ENSP00000351777.6:n.*700C>A
ENST00000448530.6:c.*700C>A	ENSP00000392088.2:n.*700C>A
ENST00000677257.1:c.*700C>A	ENSP00000504354.1:n.*700C>A
ENST00000678018.1:c.*3092C>A	ENSP00000503811.1:n.*3092C>A
ENST00000678465.1:c.*2133C>A	ENSP00000504259.1:n.*2133C>A
ENST00000678650.1:c.*700C>A	ENSP00000503426.1:n.*700C>A
ENST00000679800.1:n.3520C>A
ENST00000679902.1:c.*955C>A	ENSP00000506338.1:n.*955C>A
ENST00000681537.1:c.950C>A	ENSP00000505847.1:n.950C>A
ENST00000358901.10:c.*700C>A	ENSP00000351777.6:n.*700C>A
NM_007126.3:c.*700C>A , LRG_657t1:c.*700C>A	NP_009057.1:n.*700C>A
NM_001354927.1:c.*700C>A	NP_001341856.1:n.*700C>A
NM_001354928.1:c.*700C>A	NP_001341857.1:n.*700C>A
NM_007126.4:c.*700C>A	NP_009057.1:n.*700C>A
NM_007126.5:c.*700C>A MANE Select	NP_009057.1:n.*700C>A
NM_001354927.2:c.*700C>A	NP_001341856.1:n.*700C>A
NM_001354928.2:c.*700C>A	NP_001341857.1:n.*700C>A