Allele Registry

Canonical Allele Identifier: CA10576823

Gene: VCL HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr10:g.74074790dupG

GRCh37 chr10:g.75834548dupG

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000221392

ClinVar Variation:

228312

dbSNP:

876657674

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74074790dup , CM000672.2:g.74074790dup	GRCh38
NC_000010.10:g.75834548dup , CM000672.1:g.75834548dup	GRCh37
NC_000010.9:g.75504554dup	NCBI36
NG_008868.1:g.81677dup , LRG_383:g.81677dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.670dup MANE Select	ENSP00000211998.5:p.Glu224GlyfsTer17
ENST00000211998.8:c.670dup	ENSP00000211998.4:p.Glu224GlyfsTer17
ENST00000372755.7:c.670dup	ENSP00000361841.3:p.Glu224GlyfsTer17
ENST00000478896.2:n.332-26264dup
ENST00000623461.3:n.628dup
ENST00000624354.3:c.*425dup	ENSP00000485551.1:n.*425dup
NM_003373.3:c.670dup	NP_003364.1:p.Glu224GlyfsTer17
NM_014000.2:c.670dup , LRG_383t1:c.670dup	NP_054706.1:p.Glu224GlyfsTer17
XM_005270142.1:c.670dup	XP_005270199.1:p.Glu224GlyfsTer17
XM_005270143.1:c.670dup	XP_005270200.1:p.Glu224GlyfsTer17
NM_003373.4:c.670dup	NP_003364.1:p.Glu224GlyfsTer17
NM_014000.3:c.670dup MANE Select	NP_054706.1:p.Glu224GlyfsTer17

Search 100 bp 5'

Search 100 bp 3'