Canonical Allele Identifier: CA1757785057

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952713C= , CM000670.2:g.1952713C=	GRCh38
NC_000008.10:g.1900879C= , CM000670.1:g.1900879C=	GRCh37
NC_000008.9:g.1888286C=	NCBI36
NG_008480.1:g.133731C= , LRG_234:g.133731C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.3406C= MANE Select	ENSP00000340297.3:p.Arg1136=
ENST00000635773.1:c.3934C=
ENST00000635855.1:c.*3360C=	ENSP00000489726.1:n.*3360C=
ENST00000349830.7:c.3406C=	ENSP00000340297.3:p.Arg1136=
ENST00000398564.5:c.3481C=	ENSP00000381571.1:p.Arg1161=
ENST00000518288.5:c.3478C=	ENSP00000431012.1:p.Arg1160=
ENST00000520359.5:c.3292C=	ENSP00000427909.1:p.Arg1098=
ENST00000521927.1:n.243C=
ENST00000522435.5:c.2338C=	ENSP00000427768.1:p.Arg780=
ENST00000523596.5:n.498C=
NM_001308152.1:c.3292C=	NP_001295081.1:p.Arg1098=
NM_001308153.1:c.3478C=	NP_001295082.1:p.Arg1160=
NM_014629.2:c.3406C= , LRG_234t1:c.3406C=	NP_055444.2:p.Arg1136=
NM_014629.3:c.3406C=	NP_055444.2:p.Arg1136=
XM_005266041.2:c.3409C=	XP_005266098.1:p.Arg1137=
XM_011534766.1:c.3322C=	XP_011533068.1:p.Arg1108=
XM_011534767.1:c.3289C=	XP_011533069.1:p.Arg1097=
XM_011534768.1:c.3401-4036C=	XP_011533070.1:n.3401-4036C=
XM_011534769.1:c.3364C=	XP_011533071.1:p.Arg1122=
XM_005266041.4:c.3409C=	XP_005266098.1:p.Arg1137=
XM_011534767.2:c.3289C=	XP_011533069.1:p.Arg1097=
XM_017014003.1:c.3481C=	XP_016869492.1:p.Arg1161=
XM_024447334.1:c.3409C=	XP_024303102.1:p.Arg1137=
XM_024447335.1:c.3493C=	XP_024303103.1:p.Arg1165=
NM_014629.4:c.3406C= MANE Select	NP_055444.2:p.Arg1136=
NM_001308152.2:c.3292C=	NP_001295081.1:p.Arg1098=
NM_001308153.2:c.3478C=	NP_001295082.1:p.Arg1160=