Canonical Allele Identifier: CA373287295

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35064287T>C , CM000671.2:g.35064287T>C	GRCh38
NC_000009.11:g.35064284T>C , CM000671.1:g.35064284T>C	GRCh37
NC_000009.10:g.35054284T>C	NCBI36
NG_007887.1:g.13456A>G , LRG_657:g.13456A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.577-2A>G MANE Select	NP_009057.1:n.577-2A>G
ENST00000358901.11:c.577-2A>G MANE Select	ENSP00000351777.6:n.577-2A>G
NM_001354927.1:c.442-2A>G	NP_001341856.1:n.442-2A>G
NM_001354927.2:c.442-2A>G	NP_001341856.1:n.442-2A>G
NM_001354928.1:c.442-2A>G	NP_001341857.1:n.442-2A>G
NM_001354928.2:c.442-2A>G	NP_001341857.1:n.442-2A>G
NM_007126.3:c.577-2A>G , LRG_657t1:c.577-2A>G	NP_009057.1:n.577-2A>G
NM_007126.4:c.577-2A>G	NP_009057.1:n.577-2A>G
ENST00000358901.10:c.577-2A>G	ENSP00000351777.6:n.577-2A>G
ENST00000417448.2:c.442-2A>G	ENSP00000399456.2:n.442-2A>G
ENST00000448530.5:c.442-2A>G	ENSP00000392088.1:n.442-2A>G
ENST00000448530.6:c.442-2A>G	ENSP00000392088.2:n.442-2A>G
ENST00000480327.2:n.849-2A>G
ENST00000493886.5:n.773-2A>G
ENST00000676836.2:n.923-2A>G
ENST00000677257.1:c.571-2A>G	ENSP00000504354.1:n.571-2A>G
ENST00000678018.1:c.*548-2A>G	ENSP00000503811.1:n.*548-2A>G
ENST00000678465.1:c.577-2A>G	ENSP00000504259.1:n.577-2A>G
ENST00000678650.1:c.442-2A>G	ENSP00000503426.1:n.442-2A>G
ENST00000679204.2:c.577-2A>G	ENSP00000503131.2:n.577-2A>G
ENST00000679599.1:n.847-2A>G
ENST00000679647.1:c.577-2A>G	ENSP00000506216.1:n.577-2A>G
ENST00000679800.1:n.898-2A>G
ENST00000679862.1:c.442-2A>G	ENSP00000504990.1:n.442-2A>G
ENST00000679902.1:c.577-2A>G	ENSP00000506338.1:n.577-2A>G
ENST00000680520.1:c.229-2A>G
ENST00000680731.1:c.*65-2A>G	ENSP00000505497.1:n.*65-2A>G
ENST00000680834.1:c.58+964A>G
ENST00000680916.1:c.577-2A>G	ENSP00000505769.1:n.577-2A>G
ENST00000681335.1:c.577-2A>G	ENSP00000505230.1:n.577-2A>G
ENST00000681690.1:n.849-2A>G
ENST00000681789.1:c.136-8A>G