Canonical Allele Identifier: CA373289624

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35065361C>T , CM000671.2:g.35065361C>T	GRCh38
NC_000009.11:g.35065358C>T , CM000671.1:g.35065358C>T	GRCh37
NC_000009.10:g.35055358C>T	NCBI36
NG_007887.1:g.12382G>A , LRG_657:g.12382G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.466G>A MANE Select	NP_009057.1:p.Gly156Ser
ENST00000358901.11:c.466G>A MANE Select	ENSP00000351777.6:p.Gly156Ser
NM_001354927.1:c.331G>A	NP_001341856.1:p.Gly111Ser
NM_001354927.2:c.331G>A	NP_001341856.1:p.Gly111Ser
NM_001354928.1:c.331G>A	NP_001341857.1:p.Gly111Ser
NM_001354928.2:c.331G>A	NP_001341857.1:p.Gly111Ser
NM_007126.3:c.466G>A , LRG_657t1:c.466G>A	NP_009057.1:p.Gly156Ser
NM_007126.4:c.466G>A	NP_009057.1:p.Gly156Ser
ENST00000358901.10:c.466G>A	ENSP00000351777.6:p.Gly156Ser
ENST00000417448.1:c.331G>A	ENSP00000399456.1:p.Gly111Ser
ENST00000417448.2:c.331G>A	ENSP00000399456.2:p.Gly111Ser
ENST00000448530.5:c.331G>A	ENSP00000392088.1:p.Gly111Ser
ENST00000448530.6:c.331G>A	ENSP00000392088.2:p.Gly111Ser
ENST00000480327.2:n.738G>A
ENST00000493886.5:n.662G>A
ENST00000676836.2:n.812G>A
ENST00000677257.1:c.460G>A	ENSP00000504354.1:p.Gly154Ser
ENST00000678018.1:c.*437G>A	ENSP00000503811.1:n.*437G>A
ENST00000678465.1:c.466G>A	ENSP00000504259.1:p.Gly156Ser
ENST00000678650.1:c.331G>A	ENSP00000503426.1:p.Gly111Ser
ENST00000679204.2:c.466G>A	ENSP00000503131.2:p.Gly156Ser
ENST00000679599.1:n.736G>A
ENST00000679647.1:c.466G>A	ENSP00000506216.1:p.Gly156Ser
ENST00000679800.1:n.787G>A
ENST00000679862.1:c.331G>A	ENSP00000504990.1:p.Gly111Ser
ENST00000679902.1:c.466G>A	ENSP00000506338.1:p.Gly156Ser
ENST00000680520.1:c.21G>A
ENST00000680731.1:c.188G>A	ENSP00000505497.1:p.Trp63Ter
ENST00000680916.1:c.466G>A	ENSP00000505769.1:p.Gly156Ser
ENST00000681335.1:c.466G>A	ENSP00000505230.1:p.Gly156Ser
ENST00000681562.1:c.218G>A
ENST00000681690.1:n.738G>A
ENST00000681789.1:c.21G>A
ENST00000681845.1:c.632G>A