Canonical Allele Identifier: CA10629974

Gene: VCP

Linked Data

• ClinVar Variation Id: 366709
• ClinVar RCV Id: RCV000309265 ; RCV000390511
• dbSNP Id: rs532445930
• gnomAD v2: 9-35056729-TA-T
• gnomAD v3: 9-35056732-TA-T
• gnomAD v4: 9-35056732-TA-T
• MyVariant Identifiers: chr9:g.35056730del (hg19) ; chr9:g.35056733del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35056733del , CM000671.2:g.35056733del	GRCh38
NC_000009.11:g.35056730del , CM000671.1:g.35056730del	GRCh37
NC_000009.10:g.35046730del	NCBI36
NG_007887.1:g.21010del , LRG_657:g.21010del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.*384del MANE Select	ENSP00000351777.6:n.*384del
ENST00000417448.2:c.*384del	ENSP00000399456.2:n.*384del
ENST00000448530.6:c.*384del	ENSP00000392088.2:n.*384del
ENST00000676836.2:n.3548del
ENST00000677257.1:c.*384del	ENSP00000504354.1:n.*384del
ENST00000678018.1:c.*2776del	ENSP00000503811.1:n.*2776del
ENST00000678465.1:c.*1817del	ENSP00000504259.1:n.*1817del
ENST00000678650.1:c.*384del	ENSP00000503426.1:n.*384del
ENST00000679204.2:c.*1446del	ENSP00000503131.2:n.*1446del
ENST00000679599.1:n.5394del
ENST00000679647.1:c.*244del	ENSP00000506216.1:n.*244del
ENST00000679800.1:n.3204del
ENST00000679862.1:c.*384del	ENSP00000504990.1:n.*384del
ENST00000679902.1:c.*639del	ENSP00000506338.1:n.*639del
ENST00000680916.1:c.*770del	ENSP00000505769.1:n.*770del
ENST00000681335.1:c.*384del	ENSP00000505230.1:n.*384del
ENST00000681537.1:c.634del	ENSP00000505847.1:n.634del
ENST00000681690.1:n.4610del
ENST00000358901.10:c.*384del	ENSP00000351777.6:n.*384del
NM_007126.3:c.*384del , LRG_657t1:c.*384del	NP_009057.1:n.*384del
NM_001354927.1:c.*384del	NP_001341856.1:n.*384del
NM_001354928.1:c.*384del	NP_001341857.1:n.*384del
NM_007126.4:c.*384del	NP_009057.1:n.*384del
NM_007126.5:c.*384del MANE Select	NP_009057.1:n.*384del
NM_001354927.2:c.*384del	NP_001341856.1:n.*384del
NM_001354928.2:c.*384del	NP_001341857.1:n.*384del