Canonical Allele Identifier: CA369957308

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1450135407
• gnomAD v2: 8-1900877-A-G
• gnomAD v4: 8-1952711-A-G
• MyVariant Identifiers: chr8:g.1900877A>G (hg19) ; chr8:g.1952711A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952711A>G , CM000670.2:g.1952711A>G	GRCh38
NC_000008.10:g.1900877A>G , CM000670.1:g.1900877A>G	GRCh37
NC_000008.9:g.1888284A>G	NCBI36
NG_008480.1:g.133729A>G , LRG_234:g.133729A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3404A>G MANE Select	ENSP00000340297.3:p.Gln1135Arg
ENST00000635773.1:c.3932A>G
ENST00000635855.1:c.*3358A>G	ENSP00000489726.1:n.*3358A>G
ENST00000349830.7:c.3404A>G	ENSP00000340297.3:p.Gln1135Arg
ENST00000398564.5:c.3479A>G	ENSP00000381571.1:p.Gln1160Arg
ENST00000518288.5:c.3476A>G	ENSP00000431012.1:p.Gln1159Arg
ENST00000520359.5:c.3290A>G	ENSP00000427909.1:p.Gln1097Arg
ENST00000521927.1:n.241A>G
ENST00000522435.5:c.2336A>G	ENSP00000427768.1:p.Gln779Arg
ENST00000523596.5:n.496A>G
NM_001308152.1:c.3290A>G	NP_001295081.1:p.Gln1097Arg
NM_001308153.1:c.3476A>G	NP_001295082.1:p.Gln1159Arg
NM_014629.2:c.3404A>G , LRG_234t1:c.3404A>G	NP_055444.2:p.Gln1135Arg
NM_014629.3:c.3404A>G	NP_055444.2:p.Gln1135Arg
XM_005266041.2:c.3407A>G	XP_005266098.1:p.Gln1136Arg
XM_011534766.1:c.3320A>G	XP_011533068.1:p.Gln1107Arg
XM_011534767.1:c.3287A>G	XP_011533069.1:p.Gln1096Arg
XM_011534768.1:c.3401-4038A>G	XP_011533070.1:n.3401-4038A>G
XM_011534769.1:c.3362A>G	XP_011533071.1:p.Gln1121Arg
XM_005266041.4:c.3407A>G	XP_005266098.1:p.Gln1136Arg
XM_011534767.2:c.3287A>G	XP_011533069.1:p.Gln1096Arg
XM_017014003.1:c.3479A>G	XP_016869492.1:p.Gln1160Arg
XM_024447334.1:c.3407A>G	XP_024303102.1:p.Gln1136Arg
XM_024447335.1:c.3491A>G	XP_024303103.1:p.Gln1164Arg
NM_014629.4:c.3404A>G MANE Select	NP_055444.2:p.Gln1135Arg
NM_001308152.2:c.3290A>G	NP_001295081.1:p.Gln1097Arg
NM_001308153.2:c.3476A>G	NP_001295082.1:p.Gln1159Arg