Canonical Allele Identifier: CA1757725861

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858061C= , CM000670.2:g.1858061C=	GRCh38
NC_000008.10:g.1806227C= , CM000670.1:g.1806227C=	GRCh37
NC_000008.9:g.1793634C=	NCBI36
NG_008480.1:g.39079C= , LRG_234:g.39079C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.139C= MANE Select	ENSP00000340297.3:p.Pro47=
ENST00000635773.1:c.598C=
ENST00000635855.1:c.*90C=	ENSP00000489726.1:n.*90C=
ENST00000636175.1:c.529C=
ENST00000349830.7:c.139C=	ENSP00000340297.3:p.Pro47=
ENST00000398564.5:c.211C=	ENSP00000381571.1:p.Pro71=
ENST00000518288.5:c.211C=	ENSP00000431012.1:p.Pro71=
ENST00000520359.5:c.139C=	ENSP00000427909.1:p.Pro47=
NM_001308152.1:c.139C=	NP_001295081.1:p.Pro47=
NM_001308153.1:c.211C=	NP_001295082.1:p.Pro71=
NM_014629.2:c.139C= , LRG_234t1:c.139C=	NP_055444.2:p.Pro47=
NM_014629.3:c.139C=	NP_055444.2:p.Pro47=
XM_005266041.2:c.139C=	XP_005266098.1:p.Pro47=
XM_011534766.1:c.139C=	XP_011533068.1:p.Pro47=
XM_011534767.1:c.139C=	XP_011533069.1:p.Pro47=
XM_011534768.1:c.139C=	XP_011533070.1:p.Pro47=
XM_011534769.1:c.94C=	XP_011533071.1:p.Pro32=
XM_011534770.1:c.139C=	XP_011533072.1:p.Pro47=
XM_005266041.4:c.139C=	XP_005266098.1:p.Pro47=
XM_011534767.2:c.139C=	XP_011533069.1:p.Pro47=
XM_011534770.2:c.139C=	XP_011533072.1:p.Pro47=
XM_017014003.1:c.211C=	XP_016869492.1:p.Pro71=
XM_024447334.1:c.139C=	XP_024303102.1:p.Pro47=
XM_024447335.1:c.223C=	XP_024303103.1:p.Pro75=
NM_014629.4:c.139C= MANE Select	NP_055444.2:p.Pro47=
NM_001308152.2:c.139C=	NP_001295081.1:p.Pro47=
NM_001308153.2:c.211C=	NP_001295082.1:p.Pro71=