Canonical Allele Identifier: CA10629990

Gene: VCP

Linked Data

• ClinVar Variation Id: 366723
• ClinVar RCV Id: RCV000360664 ; RCV000407512
• dbSNP Id: rs886063893
• gnomAD v2: 9-35072565-T-C
• gnomAD v3: 9-35072568-T-C
• gnomAD v4: 9-35072568-T-C
• MyVariant Identifiers: chr9:g.35072565T>C (hg19) ; chr9:g.35072565_35072571delinsCGGCAGC (hg19) ; chr9:g.35072568T>C (hg38) ; chr9:g.35072568_35072574delinsCGGCAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35072568T>C , CM000671.2:g.35072568T>C	GRCh38
NC_000009.11:g.35072565T>C , CM000671.1:g.35072565T>C	GRCh37
NC_000009.10:g.35062565T>C	NCBI36
NG_007312.1:g.12449A>G , LRG_499:g.12449A>G
NG_007887.1:g.5175A>G , LRG_657:g.5175A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000358901.11:c.-215A>G MANE Select	ENSP00000351777.6:n.-215A>G
ENST00000448530.6:c.-410A>G	ENSP00000392088.2:n.-410A>G
ENST00000480327.2:n.58A>G
ENST00000676836.2:n.49A>G
ENST00000677257.1:c.-215A>G	ENSP00000504354.1:n.-215A>G
ENST00000678018.1:c.-215A>G	ENSP00000503811.1:n.-215A>G
ENST00000678465.1:c.-215A>G	ENSP00000504259.1:n.-215A>G
ENST00000679392.1:n.68A>G
ENST00000679599.1:n.56A>G
ENST00000679647.1:c.-215A>G	ENSP00000506216.1:n.-215A>G
ENST00000679800.1:n.24A>G
ENST00000679862.1:c.-350A>G	ENSP00000504990.1:n.-350A>G
ENST00000679902.1:c.-215A>G	ENSP00000506338.1:n.-215A>G
ENST00000680079.1:c.-215A>G	ENSP00000506523.1:n.-215A>G
ENST00000680108.1:n.68A>G
ENST00000680575.1:n.68A>G
ENST00000680916.1:c.-215A>G	ENSP00000505769.1:n.-215A>G
ENST00000681335.1:c.-215A>G	ENSP00000505230.1:n.-215A>G
ENST00000681386.1:c.-238A>G	ENSP00000505509.1:n.-238A>G
ENST00000681690.1:n.58A>G
ENST00000681845.1:c.183+1425A>G
ENST00000358901.10:c.-215A>G	ENSP00000351777.6:n.-215A>G
ENST00000448530.5:c.-410A>G	ENSP00000392088.1:n.-410A>G
NM_007126.3:c.-215A>G , LRG_657t1:c.-215A>G	NP_009057.1:n.-215A>G
NM_001354927.1:c.-410A>G	NP_001341856.1:n.-410A>G
NM_007126.4:c.-215A>G	NP_009057.1:n.-215A>G
NM_007126.5:c.-215A>G MANE Select	NP_009057.1:n.-215A>G
NM_001354927.2:c.-410A>G	NP_001341856.1:n.-410A>G
NM_001354928.2:c.-930A>G	NP_001341857.1:n.-930A>G