Canonical Allele Identifier: CA233138

Gene: ARHGEF10

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_014629.4:c.1013G>C MANE Select	NP_055444.2:p.Arg338Thr
ENST00000349830.8:c.1013G>C MANE Select	ENSP00000340297.3:p.Arg338Thr
NM_001308152.1:c.899G>C	NP_001295081.1:p.Arg300Thr
NM_001308152.2:c.899G>C	NP_001295081.1:p.Arg300Thr
NM_001308153.1:c.1088G>C	NP_001295082.1:p.Arg363Thr
NM_001308153.2:c.1088G>C	NP_001295082.1:p.Arg363Thr
NM_014629.2:c.1013G>C , LRG_234t1:c.1013G>C	NP_055444.2:p.Arg338Thr
NM_014629.3:c.1013G>C	NP_055444.2:p.Arg338Thr
ENST00000349830.7:c.1013G>C	ENSP00000340297.3:p.Arg338Thr
ENST00000398560.2:c.281G>C	ENSP00000381568.2:p.Arg94Thr
ENST00000398564.5:c.1088G>C	ENSP00000381571.1:p.Arg363Thr
ENST00000518288.5:c.1088G>C	ENSP00000431012.1:p.Arg363Thr
ENST00000520359.5:c.899G>C	ENSP00000427909.1:p.Arg300Thr
ENST00000520972.5:n.709G>C
ENST00000522435.5:c.32G>C	ENSP00000427768.1:p.Arg11Thr
ENST00000523711.5:n.737G>C
ENST00000635773.1:c.1541G>C
ENST00000635855.1:c.*967G>C	ENSP00000489726.1:n.*967G>C
XM_005266041.2:c.1016G>C	XP_005266098.1:p.Arg339Thr
XM_005266041.4:c.1016G>C	XP_005266098.1:p.Arg339Thr
XM_011534766.1:c.1016G>C	XP_011533068.1:p.Arg339Thr
XM_011534767.1:c.896G>C	XP_011533069.1:p.Arg299Thr
XM_011534767.2:c.896G>C	XP_011533069.1:p.Arg299Thr
XM_011534768.1:c.1016G>C	XP_011533070.1:p.Arg339Thr
XM_011534769.1:c.971G>C	XP_011533071.1:p.Arg324Thr
XM_011534770.1:c.1016G>C	XP_011533072.1:p.Arg339Thr
XM_011534770.2:c.1016G>C	XP_011533072.1:p.Arg339Thr
XM_017014003.1:c.1088G>C	XP_016869492.1:p.Arg363Thr
XM_024447334.1:c.1016G>C	XP_024303102.1:p.Arg339Thr
XM_024447335.1:c.1100G>C	XP_024303103.1:p.Arg367Thr