Canonical Allele Identifier: CA5039455

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35065385C>T , CM000671.2:g.35065385C>T	GRCh38
NC_000009.11:g.35065382C>T , CM000671.1:g.35065382C>T	GRCh37
NC_000009.10:g.35055382C>T	NCBI36
NG_007887.1:g.12358G>A , LRG_657:g.12358G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.446-4G>A MANE Select	NP_009057.1:n.446-4G>A
ENST00000358901.11:c.446-4G>A MANE Select	ENSP00000351777.6:n.446-4G>A
NM_001354927.1:c.311-4G>A	NP_001341856.1:n.311-4G>A
NM_001354927.2:c.311-4G>A	NP_001341856.1:n.311-4G>A
NM_001354928.1:c.311-4G>A	NP_001341857.1:n.311-4G>A
NM_001354928.2:c.311-4G>A	NP_001341857.1:n.311-4G>A
NM_007126.3:c.446-4G>A , LRG_657t1:c.446-4G>A	NP_009057.1:n.446-4G>A
NM_007126.4:c.446-4G>A	NP_009057.1:n.446-4G>A
ENST00000358901.10:c.446-4G>A	ENSP00000351777.6:n.446-4G>A
ENST00000417448.1:c.311-4G>A	ENSP00000399456.1:n.311-4G>A
ENST00000417448.2:c.311-4G>A	ENSP00000399456.2:n.311-4G>A
ENST00000448530.5:c.311-4G>A	ENSP00000392088.1:n.311-4G>A
ENST00000448530.6:c.311-4G>A	ENSP00000392088.2:n.311-4G>A
ENST00000480327.2:n.718-4G>A
ENST00000493886.5:n.642-4G>A
ENST00000676836.2:n.792-4G>A
ENST00000677257.1:c.440-4G>A	ENSP00000504354.1:n.440-4G>A
ENST00000678018.1:c.*417-4G>A	ENSP00000503811.1:n.*417-4G>A
ENST00000678465.1:c.446-4G>A	ENSP00000504259.1:n.446-4G>A
ENST00000678650.1:c.311-4G>A	ENSP00000503426.1:n.311-4G>A
ENST00000679204.2:c.446-4G>A	ENSP00000503131.2:n.446-4G>A
ENST00000679599.1:n.716-4G>A
ENST00000679647.1:c.446-4G>A	ENSP00000506216.1:n.446-4G>A
ENST00000679800.1:n.767-4G>A
ENST00000679862.1:c.311-4G>A	ENSP00000504990.1:n.311-4G>A
ENST00000679902.1:c.446-4G>A	ENSP00000506338.1:n.446-4G>A
ENST00000680731.1:c.168-4G>A	ENSP00000505497.1:n.168-4G>A
ENST00000680916.1:c.446-4G>A	ENSP00000505769.1:n.446-4G>A
ENST00000681335.1:c.446-4G>A	ENSP00000505230.1:n.446-4G>A
ENST00000681562.1:c.198-4G>A
ENST00000681690.1:n.718-4G>A
ENST00000681845.1:c.612-4G>A