Canonical Allele Identifier: CA373293479

Gene: VCP

Linked Data

• MyVariant Identifiers: chr9:g.35067918T>G (hg19) ; chr9:g.35067921T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067921T>G , CM000671.2:g.35067921T>G	GRCh38
NC_000009.11:g.35067918T>G , CM000671.1:g.35067918T>G	GRCh37
NC_000009.10:g.35057918T>G	NCBI36
NG_007887.1:g.9822A>C , LRG_657:g.9822A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.272A>C MANE Select	ENSP00000351777.6:p.Asn91Thr
ENST00000417448.2:c.137A>C	ENSP00000399456.2:p.Asn46Thr
ENST00000448530.6:c.137A>C	ENSP00000392088.2:p.Asn46Thr
ENST00000480327.2:n.544A>C
ENST00000676836.2:n.535A>C
ENST00000677257.1:c.266A>C	ENSP00000504354.1:p.Asn89Thr
ENST00000678018.1:c.*243A>C	ENSP00000503811.1:n.*243A>C
ENST00000678465.1:c.272A>C	ENSP00000504259.1:p.Asn91Thr
ENST00000678650.1:c.137A>C	ENSP00000503426.1:p.Asn46Thr
ENST00000679204.2:c.272A>C	ENSP00000503131.2:p.Asn91Thr
ENST00000679449.1:c.291A>C
ENST00000679599.1:n.542A>C
ENST00000679647.1:c.272A>C	ENSP00000506216.1:p.Asn91Thr
ENST00000679800.1:n.510A>C
ENST00000679862.1:c.137A>C	ENSP00000504990.1:p.Asn46Thr
ENST00000679902.1:c.272A>C	ENSP00000506338.1:p.Asn91Thr
ENST00000680079.1:c.*193A>C	ENSP00000506523.1:n.*193A>C
ENST00000680731.1:c.137A>C	ENSP00000505497.1:p.Asn46Thr
ENST00000680900.1:c.276A>C
ENST00000680916.1:c.272A>C	ENSP00000505769.1:p.Asn91Thr
ENST00000681335.1:c.272A>C	ENSP00000505230.1:p.Asn91Thr
ENST00000681386.1:c.137A>C	ENSP00000505509.1:p.Asn46Thr
ENST00000681690.1:n.544A>C
ENST00000681845.1:c.438A>C
ENST00000358901.10:c.272A>C	ENSP00000351777.6:p.Asn91Thr
ENST00000417448.1:c.137A>C	ENSP00000399456.1:p.Asn46Thr
ENST00000448530.5:c.137A>C	ENSP00000392088.1:p.Asn46Thr
ENST00000493886.5:n.468A>C
NM_007126.3:c.272A>C , LRG_657t1:c.272A>C	NP_009057.1:p.Asn91Thr
NM_001354927.1:c.137A>C	NP_001341856.1:p.Asn46Thr
NM_001354928.1:c.137A>C	NP_001341857.1:p.Asn46Thr
NM_007126.4:c.272A>C	NP_009057.1:p.Asn91Thr
NM_007126.5:c.272A>C MANE Select	NP_009057.1:p.Asn91Thr
NM_001354927.2:c.137A>C	NP_001341856.1:p.Asn46Thr
NM_001354928.2:c.137A>C	NP_001341857.1:p.Asn46Thr