Canonical Allele Identifier: CA1757727708

Gene: ARHGEF10

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_014629.4:c.1013G= MANE Select	NP_055444.2:p.Arg338=
ENST00000349830.8:c.1013G= MANE Select	ENSP00000340297.3:p.Arg338=
NM_001308152.1:c.899G=	NP_001295081.1:p.Arg300=
NM_001308152.2:c.899G=	NP_001295081.1:p.Arg300=
NM_001308153.1:c.1088G=	NP_001295082.1:p.Arg363=
NM_001308153.2:c.1088G=	NP_001295082.1:p.Arg363=
NM_014629.2:c.1013G= , LRG_234t1:c.1013G=	NP_055444.2:p.Arg338=
NM_014629.3:c.1013G=	NP_055444.2:p.Arg338=
ENST00000349830.7:c.1013G=	ENSP00000340297.3:p.Arg338=
ENST00000398560.2:c.281G=	ENSP00000381568.2:p.Arg94=
ENST00000398564.5:c.1088G=	ENSP00000381571.1:p.Arg363=
ENST00000518288.5:c.1088G=	ENSP00000431012.1:p.Arg363=
ENST00000520359.5:c.899G=	ENSP00000427909.1:p.Arg300=
ENST00000520972.5:n.709G=
ENST00000522435.5:c.32G=	ENSP00000427768.1:p.Arg11=
ENST00000523711.5:n.737G=
ENST00000635773.1:c.1541G=
ENST00000635855.1:c.*967G=	ENSP00000489726.1:n.*967G=
XM_005266041.2:c.1016G=	XP_005266098.1:p.Arg339=
XM_005266041.4:c.1016G=	XP_005266098.1:p.Arg339=
XM_011534766.1:c.1016G=	XP_011533068.1:p.Arg339=
XM_011534767.1:c.896G=	XP_011533069.1:p.Arg299=
XM_011534767.2:c.896G=	XP_011533069.1:p.Arg299=
XM_011534768.1:c.1016G=	XP_011533070.1:p.Arg339=
XM_011534769.1:c.971G=	XP_011533071.1:p.Arg324=
XM_011534770.1:c.1016G=	XP_011533072.1:p.Arg339=
XM_011534770.2:c.1016G=	XP_011533072.1:p.Arg339=
XM_017014003.1:c.1088G=	XP_016869492.1:p.Arg363=
XM_024447334.1:c.1016G=	XP_024303102.1:p.Arg339=
XM_024447335.1:c.1100G=	XP_024303103.1:p.Arg367=