Canonical Allele Identifier: CA373269685

Gene: VCP

Linked Data

• ClinVar Variation Id: 940463
• ClinVar RCV Id: RCV001210057
• dbSNP Id: rs1828632660
• MyVariant Identifiers: chr9:g.35057446T>A (hg19) ; chr9:g.35057449T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35057449T>A , CM000671.2:g.35057449T>A	GRCh38
NC_000009.11:g.35057446T>A , CM000671.1:g.35057446T>A	GRCh37
NC_000009.10:g.35047446T>A	NCBI36
NG_007887.1:g.20294A>T , LRG_657:g.20294A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.2242A>T MANE Select	ENSP00000351777.6:p.Ser748Cys
ENST00000417448.2:c.2107A>T	ENSP00000399456.2:p.Ser703Cys
ENST00000448530.6:c.2107A>T	ENSP00000392088.2:p.Ser703Cys
ENST00000479300.2:n.770A>T
ENST00000676836.2:n.2985A>T
ENST00000677257.1:c.2236A>T	ENSP00000504354.1:p.Ser746Cys
ENST00000678018.1:c.*2213A>T	ENSP00000503811.1:n.*2213A>T
ENST00000678465.1:c.*1254A>T	ENSP00000504259.1:n.*1254A>T
ENST00000678650.1:c.2107A>T	ENSP00000503426.1:p.Ser703Cys
ENST00000679204.2:c.*883A>T	ENSP00000503131.2:n.*883A>T
ENST00000679599.1:n.4831A>T
ENST00000679647.1:c.2084-354A>T	ENSP00000506216.1:n.2084-354A>T
ENST00000679800.1:n.2641A>T
ENST00000679862.1:c.2104A>T	ENSP00000504990.1:p.Ser702Cys
ENST00000679902.1:c.2242A>T	ENSP00000506338.1:p.Ser748Cys
ENST00000680916.1:c.*207A>T	ENSP00000505769.1:n.*207A>T
ENST00000681335.1:c.2086A>T	ENSP00000505230.1:p.Ser696Cys
ENST00000681537.1:c.82A>T	ENSP00000505847.1:p.Ser28Cys
ENST00000681690.1:n.4047A>T
ENST00000358901.10:c.2242A>T	ENSP00000351777.6:p.Ser748Cys
ENST00000466100.1:n.385A>T
ENST00000493886.5:n.2516A>T
NM_007126.3:c.2242A>T , LRG_657t1:c.2242A>T	NP_009057.1:p.Ser748Cys
NM_001354927.1:c.2107A>T	NP_001341856.1:p.Ser703Cys
NM_001354928.1:c.2107A>T	NP_001341857.1:p.Ser703Cys
NM_007126.4:c.2242A>T	NP_009057.1:p.Ser748Cys
NM_007126.5:c.2242A>T MANE Select	NP_009057.1:p.Ser748Cys
NM_001354927.2:c.2107A>T	NP_001341856.1:p.Ser703Cys
NM_001354928.2:c.2107A>T	NP_001341857.1:p.Ser703Cys