Canonical Allele Identifier: CA5039492

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35066736A>G , CM000671.2:g.35066736A>G	GRCh38
NC_000009.11:g.35066733A>G , CM000671.1:g.35066733A>G	GRCh37
NC_000009.10:g.35056733A>G	NCBI36
NG_007887.1:g.11007T>C , LRG_657:g.11007T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.384T>C MANE Select	NP_009057.1:p.Gly128=
ENST00000358901.11:c.384T>C MANE Select	ENSP00000351777.6:p.Gly128=
NM_001354927.1:c.249T>C	NP_001341856.1:p.Gly83=
NM_001354927.2:c.249T>C	NP_001341856.1:p.Gly83=
NM_001354928.1:c.249T>C	NP_001341857.1:p.Gly83=
NM_001354928.2:c.249T>C	NP_001341857.1:p.Gly83=
NM_007126.3:c.384T>C , LRG_657t1:c.384T>C	NP_009057.1:p.Gly128=
NM_007126.4:c.384T>C	NP_009057.1:p.Gly128=
ENST00000358901.10:c.384T>C	ENSP00000351777.6:p.Gly128=
ENST00000417448.1:c.249T>C	ENSP00000399456.1:p.Gly83=
ENST00000417448.2:c.249T>C	ENSP00000399456.2:p.Gly83=
ENST00000448530.5:c.249T>C	ENSP00000392088.1:p.Gly83=
ENST00000448530.6:c.249T>C	ENSP00000392088.2:p.Gly83=
ENST00000480327.2:n.656T>C
ENST00000493886.5:n.580T>C
ENST00000676836.2:n.730T>C
ENST00000677257.1:c.378T>C	ENSP00000504354.1:p.Gly126=
ENST00000678018.1:c.*355T>C	ENSP00000503811.1:n.*355T>C
ENST00000678465.1:c.384T>C	ENSP00000504259.1:p.Gly128=
ENST00000678650.1:c.249T>C	ENSP00000503426.1:p.Gly83=
ENST00000679204.2:c.384T>C	ENSP00000503131.2:p.Gly128=
ENST00000679599.1:n.654T>C
ENST00000679647.1:c.384T>C	ENSP00000506216.1:p.Gly128=
ENST00000679800.1:n.705T>C
ENST00000679862.1:c.249T>C	ENSP00000504990.1:p.Gly83=
ENST00000679902.1:c.384T>C	ENSP00000506338.1:p.Gly128=
ENST00000680079.1:c.*305T>C	ENSP00000506523.1:n.*305T>C
ENST00000680731.1:c.167+1155T>C	ENSP00000505497.1:n.167+1155T>C
ENST00000680916.1:c.384T>C	ENSP00000505769.1:p.Gly128=
ENST00000681335.1:c.384T>C	ENSP00000505230.1:p.Gly128=
ENST00000681562.1:c.82T>C
ENST00000681690.1:n.656T>C
ENST00000681845.1:c.550T>C