Canonical Allele Identifier: CA5039057

Gene: VCP

Linked Data

• ClinVar Variation Id: 284304
• ClinVar RCV Id: RCV000291446 ; RCV000301970 ; RCV000376145 ; RCV001252622 ; RCV001559813
• dbSNP Id: rs201091341
• ExAC: 9:35057110 C / A
• gnomAD v2: 9-35057110-C-A
• gnomAD v3: 9-35057113-C-A
• gnomAD v4: 9-35057113-C-A
• MyVariant Identifiers: chr9:g.35057110C>A (hg19) ; chr9:g.35057113C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35057113C>A , CM000671.2:g.35057113C>A	GRCh38
NC_000009.11:g.35057110C>A , CM000671.1:g.35057110C>A	GRCh37
NC_000009.10:g.35047110C>A	NCBI36
NG_007887.1:g.20630G>T , LRG_657:g.20630G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.*4G>T MANE Select	ENSP00000351777.6:n.*4G>T
ENST00000417448.2:c.*4G>T	ENSP00000399456.2:n.*4G>T
ENST00000448530.6:c.*4G>T	ENSP00000392088.2:n.*4G>T
ENST00000479300.2:n.953G>T
ENST00000676836.2:n.3168G>T
ENST00000677257.1:c.*4G>T	ENSP00000504354.1:n.*4G>T
ENST00000678018.1:c.*2396G>T	ENSP00000503811.1:n.*2396G>T
ENST00000678465.1:c.*1437G>T	ENSP00000504259.1:n.*1437G>T
ENST00000678650.1:c.*4G>T	ENSP00000503426.1:n.*4G>T
ENST00000679204.2:c.*1066G>T	ENSP00000503131.2:n.*1066G>T
ENST00000679599.1:n.5014G>T
ENST00000679647.1:c.2084-18G>T	ENSP00000506216.1:n.2084-18G>T
ENST00000679800.1:n.2824G>T
ENST00000679862.1:c.*4G>T	ENSP00000504990.1:n.*4G>T
ENST00000679902.1:c.*259G>T	ENSP00000506338.1:n.*259G>T
ENST00000680916.1:c.*390G>T	ENSP00000505769.1:n.*390G>T
ENST00000681335.1:c.*4G>T	ENSP00000505230.1:n.*4G>T
ENST00000681537.1:c.254G>T	ENSP00000505847.1:n.254G>T
ENST00000681690.1:n.4230G>T
ENST00000358901.10:c.*4G>T	ENSP00000351777.6:n.*4G>T
ENST00000493886.5:n.2699G>T
NM_007126.3:c.*4G>T , LRG_657t1:c.*4G>T	NP_009057.1:n.*4G>T
NM_001354927.1:c.*4G>T	NP_001341856.1:n.*4G>T
NM_001354928.1:c.*4G>T	NP_001341857.1:n.*4G>T
NM_007126.4:c.*4G>T	NP_009057.1:n.*4G>T
NM_007126.5:c.*4G>T MANE Select	NP_009057.1:n.*4G>T
NM_001354927.2:c.*4G>T	NP_001341856.1:n.*4G>T
NM_001354928.2:c.*4G>T	NP_001341857.1:n.*4G>T