Canonical Allele Identifier: CA369956932

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1882687G>A , CM000670.2:g.1882687G>A	GRCh38
NC_000008.10:g.1830853G>A , CM000670.1:g.1830853G>A	GRCh37
NC_000008.9:g.1818260G>A	NCBI36
NG_008480.1:g.63705G>A , LRG_234:g.63705G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014629.4:c.1013G>A MANE Select	NP_055444.2:p.Arg338Lys
ENST00000349830.8:c.1013G>A MANE Select	ENSP00000340297.3:p.Arg338Lys
NM_001308152.1:c.899G>A	NP_001295081.1:p.Arg300Lys
NM_001308152.2:c.899G>A	NP_001295081.1:p.Arg300Lys
NM_001308153.1:c.1088G>A	NP_001295082.1:p.Arg363Lys
NM_001308153.2:c.1088G>A	NP_001295082.1:p.Arg363Lys
NM_014629.2:c.1013G>A , LRG_234t1:c.1013G>A	NP_055444.2:p.Arg338Lys
NM_014629.3:c.1013G>A	NP_055444.2:p.Arg338Lys
ENST00000349830.7:c.1013G>A	ENSP00000340297.3:p.Arg338Lys
ENST00000398560.2:c.281G>A	ENSP00000381568.2:p.Arg94Lys
ENST00000398564.5:c.1088G>A	ENSP00000381571.1:p.Arg363Lys
ENST00000518288.5:c.1088G>A	ENSP00000431012.1:p.Arg363Lys
ENST00000520359.5:c.899G>A	ENSP00000427909.1:p.Arg300Lys
ENST00000520972.5:n.709G>A
ENST00000522435.5:c.32G>A	ENSP00000427768.1:p.Arg11Lys
ENST00000523711.5:n.737G>A
ENST00000635773.1:c.1541G>A
ENST00000635855.1:c.*967G>A	ENSP00000489726.1:n.*967G>A
XM_005266041.2:c.1016G>A	XP_005266098.1:p.Arg339Lys
XM_005266041.4:c.1016G>A	XP_005266098.1:p.Arg339Lys
XM_011534766.1:c.1016G>A	XP_011533068.1:p.Arg339Lys
XM_011534767.1:c.896G>A	XP_011533069.1:p.Arg299Lys
XM_011534767.2:c.896G>A	XP_011533069.1:p.Arg299Lys
XM_011534768.1:c.1016G>A	XP_011533070.1:p.Arg339Lys
XM_011534769.1:c.971G>A	XP_011533071.1:p.Arg324Lys
XM_011534770.1:c.1016G>A	XP_011533072.1:p.Arg339Lys
XM_011534770.2:c.1016G>A	XP_011533072.1:p.Arg339Lys
XM_017014003.1:c.1088G>A	XP_016869492.1:p.Arg363Lys
XM_024447334.1:c.1016G>A	XP_024303102.1:p.Arg339Lys
XM_024447335.1:c.1100G>A	XP_024303103.1:p.Arg367Lys