Canonical Allele Identifier: CA373293689

Gene: VCP

Linked Data

• gnomAD v4: 9-35067941-C-G
• MyVariant Identifiers: chr9:g.35067938C>G (hg19) ; chr9:g.35067941C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067941C>G , CM000671.2:g.35067941C>G	GRCh38
NC_000009.11:g.35067938C>G , CM000671.1:g.35067938C>G	GRCh37
NC_000009.10:g.35057938C>G	NCBI36
NG_007887.1:g.9802G>C , LRG_657:g.9802G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.252G>C MANE Select	ENSP00000351777.6:p.Met84Ile
ENST00000417448.2:c.117G>C	ENSP00000399456.2:p.Met39Ile
ENST00000448530.6:c.117G>C	ENSP00000392088.2:p.Met39Ile
ENST00000480327.2:n.524G>C
ENST00000676836.2:n.515G>C
ENST00000677257.1:c.246G>C	ENSP00000504354.1:p.Met82Ile
ENST00000678018.1:c.*223G>C	ENSP00000503811.1:n.*223G>C
ENST00000678465.1:c.252G>C	ENSP00000504259.1:p.Met84Ile
ENST00000678650.1:c.117G>C	ENSP00000503426.1:p.Met39Ile
ENST00000679204.2:c.252G>C	ENSP00000503131.2:p.Met84Ile
ENST00000679449.1:c.271G>C
ENST00000679599.1:n.522G>C
ENST00000679647.1:c.252G>C	ENSP00000506216.1:p.Met84Ile
ENST00000679800.1:n.490G>C
ENST00000679862.1:c.117G>C	ENSP00000504990.1:p.Met39Ile
ENST00000679902.1:c.252G>C	ENSP00000506338.1:p.Met84Ile
ENST00000680079.1:c.*173G>C	ENSP00000506523.1:n.*173G>C
ENST00000680731.1:c.117G>C	ENSP00000505497.1:p.Met39Ile
ENST00000680900.1:c.256G>C
ENST00000680916.1:c.252G>C	ENSP00000505769.1:p.Met84Ile
ENST00000681335.1:c.252G>C	ENSP00000505230.1:p.Met84Ile
ENST00000681386.1:c.117G>C	ENSP00000505509.1:p.Met39Ile
ENST00000681690.1:n.524G>C
ENST00000681845.1:c.418G>C
ENST00000358901.10:c.252G>C	ENSP00000351777.6:p.Met84Ile
ENST00000417448.1:c.117G>C	ENSP00000399456.1:p.Met39Ile
ENST00000448530.5:c.117G>C	ENSP00000392088.1:p.Met39Ile
ENST00000493886.5:n.448G>C
NM_007126.3:c.252G>C , LRG_657t1:c.252G>C	NP_009057.1:p.Met84Ile
NM_001354927.1:c.117G>C	NP_001341856.1:p.Met39Ile
NM_001354928.1:c.117G>C	NP_001341857.1:p.Met39Ile
NM_007126.4:c.252G>C	NP_009057.1:p.Met84Ile
NM_007126.5:c.252G>C MANE Select	NP_009057.1:p.Met84Ile
NM_001354927.2:c.117G>C	NP_001341856.1:p.Met39Ile
NM_001354928.2:c.117G>C	NP_001341857.1:p.Met39Ile