Canonical Allele Identifier: CA373289580

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35065355T>C , CM000671.2:g.35065355T>C	GRCh38
NC_000009.11:g.35065352T>C , CM000671.1:g.35065352T>C	GRCh37
NC_000009.10:g.35055352T>C	NCBI36
NG_007887.1:g.12388A>G , LRG_657:g.12388A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.472A>G MANE Select	NP_009057.1:p.Met158Val
ENST00000358901.11:c.472A>G MANE Select	ENSP00000351777.6:p.Met158Val
NM_001354927.1:c.337A>G	NP_001341856.1:p.Met113Val
NM_001354927.2:c.337A>G	NP_001341856.1:p.Met113Val
NM_001354928.1:c.337A>G	NP_001341857.1:p.Met113Val
NM_001354928.2:c.337A>G	NP_001341857.1:p.Met113Val
NM_007126.3:c.472A>G , LRG_657t1:c.472A>G	NP_009057.1:p.Met158Val
NM_007126.4:c.472A>G	NP_009057.1:p.Met158Val
ENST00000358901.10:c.472A>G	ENSP00000351777.6:p.Met158Val
ENST00000417448.1:c.337A>G	ENSP00000399456.1:p.Met113Val
ENST00000417448.2:c.337A>G	ENSP00000399456.2:p.Met113Val
ENST00000448530.5:c.337A>G	ENSP00000392088.1:p.Met113Val
ENST00000448530.6:c.337A>G	ENSP00000392088.2:p.Met113Val
ENST00000480327.2:n.744A>G
ENST00000493886.5:n.668A>G
ENST00000676836.2:n.818A>G
ENST00000677257.1:c.466A>G	ENSP00000504354.1:p.Met156Val
ENST00000678018.1:c.*443A>G	ENSP00000503811.1:n.*443A>G
ENST00000678465.1:c.472A>G	ENSP00000504259.1:p.Met158Val
ENST00000678650.1:c.337A>G	ENSP00000503426.1:p.Met113Val
ENST00000679204.2:c.472A>G	ENSP00000503131.2:p.Met158Val
ENST00000679599.1:n.742A>G
ENST00000679647.1:c.472A>G	ENSP00000506216.1:p.Met158Val
ENST00000679800.1:n.793A>G
ENST00000679862.1:c.337A>G	ENSP00000504990.1:p.Met113Val
ENST00000679902.1:c.472A>G	ENSP00000506338.1:p.Met158Val
ENST00000680520.1:c.27A>G
ENST00000680731.1:c.194A>G	ENSP00000505497.1:p.Asp65Gly
ENST00000680916.1:c.472A>G	ENSP00000505769.1:p.Met158Val
ENST00000681335.1:c.472A>G	ENSP00000505230.1:p.Met158Val
ENST00000681562.1:c.224A>G
ENST00000681690.1:n.744A>G
ENST00000681789.1:c.27A>G
ENST00000681845.1:c.638A>G