Canonical Allele Identifier: CA170588676

Gene: ARHGEF10

Linked Data

• ClinVar Variation Id: 450742
• ClinVar RCV Id: RCV000520161
• dbSNP Id: rs1022200702
• gnomAD v2: 8-1806281-G-A
• gnomAD v3: 8-1858115-G-A
• gnomAD v4: 8-1858115-G-A
• MyVariant Identifiers: chr8:g.1806281G>A (hg19) ; chr8:g.1858115G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858115G>A , CM000670.2:g.1858115G>A	GRCh38
NC_000008.10:g.1806281G>A , CM000670.1:g.1806281G>A	GRCh37
NC_000008.9:g.1793688G>A	NCBI36
NG_008480.1:g.39133G>A , LRG_234:g.39133G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.193G>A MANE Select	ENSP00000340297.3:p.Gly65Arg
ENST00000635773.1:c.652G>A
ENST00000635855.1:c.*144G>A	ENSP00000489726.1:n.*144G>A
ENST00000636175.1:c.583G>A
ENST00000349830.7:c.193G>A	ENSP00000340297.3:p.Gly65Arg
ENST00000398564.5:c.265G>A	ENSP00000381571.1:p.Gly89Arg
ENST00000518288.5:c.265G>A	ENSP00000431012.1:p.Gly89Arg
ENST00000520359.5:c.193G>A	ENSP00000427909.1:p.Gly65Arg
NM_001308152.1:c.193G>A	NP_001295081.1:p.Gly65Arg
NM_001308153.1:c.265G>A	NP_001295082.1:p.Gly89Arg
NM_014629.2:c.193G>A , LRG_234t1:c.193G>A	NP_055444.2:p.Gly65Arg
NM_014629.3:c.193G>A	NP_055444.2:p.Gly65Arg
XM_005266041.2:c.193G>A	XP_005266098.1:p.Gly65Arg
XM_011534766.1:c.193G>A	XP_011533068.1:p.Gly65Arg
XM_011534767.1:c.193G>A	XP_011533069.1:p.Gly65Arg
XM_011534768.1:c.193G>A	XP_011533070.1:p.Gly65Arg
XM_011534769.1:c.148G>A	XP_011533071.1:p.Gly50Arg
XM_011534770.1:c.193G>A	XP_011533072.1:p.Gly65Arg
XM_005266041.4:c.193G>A	XP_005266098.1:p.Gly65Arg
XM_011534767.2:c.193G>A	XP_011533069.1:p.Gly65Arg
XM_011534770.2:c.193G>A	XP_011533072.1:p.Gly65Arg
XM_017014003.1:c.265G>A	XP_016869492.1:p.Gly89Arg
XM_024447334.1:c.193G>A	XP_024303102.1:p.Gly65Arg
XM_024447335.1:c.277G>A	XP_024303103.1:p.Gly93Arg
NM_014629.4:c.193G>A MANE Select	NP_055444.2:p.Gly65Arg
NM_001308152.2:c.193G>A	NP_001295081.1:p.Gly65Arg
NM_001308153.2:c.265G>A	NP_001295082.1:p.Gly89Arg