Canonical Allele Identifier: CA1757727673

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1882669C= , CM000670.2:g.1882669C=	GRCh38
NC_000008.10:g.1830835C= , CM000670.1:g.1830835C=	GRCh37
NC_000008.9:g.1818242C=	NCBI36
NG_008480.1:g.63687C= , LRG_234:g.63687C=

Transcript Alleles

HGVS	Amino-acid Change
NM_014629.4:c.995C= MANE Select	NP_055444.2:p.Thr332=
ENST00000349830.8:c.995C= MANE Select	ENSP00000340297.3:p.Thr332=
NM_001308152.1:c.881C=	NP_001295081.1:p.Thr294=
NM_001308152.2:c.881C=	NP_001295081.1:p.Thr294=
NM_001308153.1:c.1070C=	NP_001295082.1:p.Thr357=
NM_001308153.2:c.1070C=	NP_001295082.1:p.Thr357=
NM_014629.2:c.995C= , LRG_234t1:c.995C=	NP_055444.2:p.Thr332=
NM_014629.3:c.995C=	NP_055444.2:p.Thr332=
ENST00000349830.7:c.995C=	ENSP00000340297.3:p.Thr332=
ENST00000398560.2:c.263C=	ENSP00000381568.2:p.Thr88=
ENST00000398564.5:c.1070C=	ENSP00000381571.1:p.Thr357=
ENST00000518288.5:c.1070C=	ENSP00000431012.1:p.Thr357=
ENST00000520359.5:c.881C=	ENSP00000427909.1:p.Thr294=
ENST00000520972.5:n.691C=
ENST00000522435.5:c.14C=	ENSP00000427768.1:p.Thr5=
ENST00000523711.5:n.719C=
ENST00000635773.1:c.1523C=
ENST00000635855.1:c.*949C=	ENSP00000489726.1:n.*949C=
XM_005266041.2:c.998C=	XP_005266098.1:p.Thr333=
XM_005266041.4:c.998C=	XP_005266098.1:p.Thr333=
XM_011534766.1:c.998C=	XP_011533068.1:p.Thr333=
XM_011534767.1:c.878C=	XP_011533069.1:p.Thr293=
XM_011534767.2:c.878C=	XP_011533069.1:p.Thr293=
XM_011534768.1:c.998C=	XP_011533070.1:p.Thr333=
XM_011534769.1:c.953C=	XP_011533071.1:p.Thr318=
XM_011534770.1:c.998C=	XP_011533072.1:p.Thr333=
XM_011534770.2:c.998C=	XP_011533072.1:p.Thr333=
XM_017014003.1:c.1070C=	XP_016869492.1:p.Thr357=
XM_024447334.1:c.998C=	XP_024303102.1:p.Thr333=
XM_024447335.1:c.1082C=	XP_024303103.1:p.Thr361=