Canonical Allele Identifier: CA4599741

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1860104C>T , CM000670.2:g.1860104C>T	GRCh38
NC_000008.10:g.1808270C>T , CM000670.1:g.1808270C>T	GRCh37
NC_000008.9:g.1795677C>T	NCBI36
NG_008480.1:g.41122C>T , LRG_234:g.41122C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.401C>T MANE Select	ENSP00000340297.3:p.Ala134Val
ENST00000635773.1:c.860C>T
ENST00000635855.1:c.*352C>T	ENSP00000489726.1:n.*352C>T
ENST00000636175.1:c.791C>T
ENST00000349830.7:c.401C>T	ENSP00000340297.3:p.Ala134Val
ENST00000382795.7:n.270C>T
ENST00000398560.2:c.-218C>T	ENSP00000381568.2:n.-218C>T
ENST00000398564.5:c.473C>T	ENSP00000381571.1:p.Ala158Val
ENST00000518288.5:c.473C>T	ENSP00000431012.1:p.Ala158Val
ENST00000520359.5:c.401C>T	ENSP00000427909.1:p.Ala134Val
ENST00000520972.5:n.211C>T
ENST00000522969.1:n.190C>T
NM_001308152.1:c.401C>T	NP_001295081.1:p.Ala134Val
NM_001308153.1:c.473C>T	NP_001295082.1:p.Ala158Val
NM_014629.2:c.401C>T , LRG_234t1:c.401C>T	NP_055444.2:p.Ala134Val
NM_014629.3:c.401C>T	NP_055444.2:p.Ala134Val
XM_005266041.2:c.401C>T	XP_005266098.1:p.Ala134Val
XM_011534766.1:c.401C>T	XP_011533068.1:p.Ala134Val
XM_011534767.1:c.401C>T	XP_011533069.1:p.Ala134Val
XM_011534768.1:c.401C>T	XP_011533070.1:p.Ala134Val
XM_011534769.1:c.356C>T	XP_011533071.1:p.Ala119Val
XM_011534770.1:c.401C>T	XP_011533072.1:p.Ala134Val
XM_005266041.4:c.401C>T	XP_005266098.1:p.Ala134Val
XM_011534767.2:c.401C>T	XP_011533069.1:p.Ala134Val
XM_011534770.2:c.401C>T	XP_011533072.1:p.Ala134Val
XM_017014003.1:c.473C>T	XP_016869492.1:p.Ala158Val
XM_024447334.1:c.401C>T	XP_024303102.1:p.Ala134Val
XM_024447335.1:c.485C>T	XP_024303103.1:p.Ala162Val
NM_014629.4:c.401C>T MANE Select	NP_055444.2:p.Ala134Val
NM_001308152.2:c.401C>T	NP_001295081.1:p.Ala134Val
NM_001308153.2:c.473C>T	NP_001295082.1:p.Ala158Val