Canonical Allele Identifier: CA587568770

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35057534T>C , CM000671.2:g.35057534T>C	GRCh38
NC_000009.11:g.35057531T>C , CM000671.1:g.35057531T>C	GRCh37
NC_000009.10:g.35047531T>C	NCBI36
NG_007887.1:g.20209A>G , LRG_657:g.20209A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.2161-4A>G MANE Select	NP_009057.1:n.2161-4A>G
ENST00000358901.11:c.2161-4A>G MANE Select	ENSP00000351777.6:n.2161-4A>G
NM_001354927.1:c.2026-4A>G	NP_001341856.1:n.2026-4A>G
NM_001354927.2:c.2026-4A>G	NP_001341856.1:n.2026-4A>G
NM_001354928.1:c.2026-4A>G	NP_001341857.1:n.2026-4A>G
NM_001354928.2:c.2026-4A>G	NP_001341857.1:n.2026-4A>G
NM_007126.3:c.2161-4A>G , LRG_657t1:c.2161-4A>G	NP_009057.1:n.2161-4A>G
NM_007126.4:c.2161-4A>G	NP_009057.1:n.2161-4A>G
ENST00000358901.10:c.2161-4A>G	ENSP00000351777.6:n.2161-4A>G
ENST00000417448.2:c.2026-4A>G	ENSP00000399456.2:n.2026-4A>G
ENST00000448530.6:c.2026-4A>G	ENSP00000392088.2:n.2026-4A>G
ENST00000466100.1:n.300A>G
ENST00000479300.2:n.689-4A>G
ENST00000493886.5:n.2435-4A>G
ENST00000676836.2:n.2904-4A>G
ENST00000677257.1:c.2155-4A>G	ENSP00000504354.1:n.2155-4A>G
ENST00000678018.1:c.*2132-4A>G	ENSP00000503811.1:n.*2132-4A>G
ENST00000678465.1:c.*1173-4A>G	ENSP00000504259.1:n.*1173-4A>G
ENST00000678650.1:c.2026-4A>G	ENSP00000503426.1:n.2026-4A>G
ENST00000679204.2:c.*802-4A>G	ENSP00000503131.2:n.*802-4A>G
ENST00000679599.1:n.4746A>G
ENST00000679647.1:c.2084-439A>G	ENSP00000506216.1:n.2084-439A>G
ENST00000679800.1:n.2560-4A>G
ENST00000679862.1:c.2026-7A>G	ENSP00000504990.1:n.2026-7A>G
ENST00000679902.1:c.2161-4A>G	ENSP00000506338.1:n.2161-4A>G
ENST00000680916.1:c.*126-4A>G	ENSP00000505769.1:n.*126-4A>G
ENST00000681335.1:c.2005-4A>G	ENSP00000505230.1:n.2005-4A>G
ENST00000681690.1:n.3962A>G