Canonical Allele Identifier: CA4601074

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1928541G>A , CM000670.2:g.1928541G>A	GRCh38
NC_000008.10:g.1876707G>A , CM000670.1:g.1876707G>A	GRCh37
NC_000008.9:g.1864114G>A	NCBI36
NG_008480.1:g.109559G>A , LRG_234:g.109559G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014629.4:c.2812G>A MANE Select	NP_055444.2:p.Val938Ile
ENST00000349830.8:c.2812G>A MANE Select	ENSP00000340297.3:p.Val938Ile
NM_001308152.1:c.2698G>A	NP_001295081.1:p.Val900Ile
NM_001308152.2:c.2698G>A	NP_001295081.1:p.Val900Ile
NM_001308153.1:c.2884G>A	NP_001295082.1:p.Val962Ile
NM_001308153.2:c.2884G>A	NP_001295082.1:p.Val962Ile
NM_014629.2:c.2812G>A , LRG_234t1:c.2812G>A	NP_055444.2:p.Val938Ile
NM_014629.3:c.2812G>A	NP_055444.2:p.Val938Ile
ENST00000349830.7:c.2812G>A	ENSP00000340297.3:p.Val938Ile
ENST00000398564.5:c.2887G>A	ENSP00000381571.1:p.Val963Ile
ENST00000518288.5:c.2884G>A	ENSP00000431012.1:p.Val962Ile
ENST00000520359.5:c.2698G>A	ENSP00000427909.1:p.Val900Ile
ENST00000522435.5:c.1744G>A	ENSP00000427768.1:p.Val582Ile
ENST00000635773.1:c.3340G>A
ENST00000635855.1:c.*2766G>A	ENSP00000489726.1:n.*2766G>A
XM_005266041.2:c.2815G>A	XP_005266098.1:p.Val939Ile
XM_005266041.4:c.2815G>A	XP_005266098.1:p.Val939Ile
XM_011534766.1:c.2728G>A	XP_011533068.1:p.Val910Ile
XM_011534767.1:c.2695G>A	XP_011533069.1:p.Val899Ile
XM_011534767.2:c.2695G>A	XP_011533069.1:p.Val899Ile
XM_011534768.1:c.2815G>A	XP_011533070.1:p.Val939Ile
XM_011534769.1:c.2770G>A	XP_011533071.1:p.Val924Ile
XM_011534770.1:c.2815G>A	XP_011533072.1:p.Val939Ile
XM_011534770.2:c.2815G>A	XP_011533072.1:p.Val939Ile
XM_017014003.1:c.2887G>A	XP_016869492.1:p.Val963Ile
XM_024447334.1:c.2815G>A	XP_024303102.1:p.Val939Ile
XM_024447335.1:c.2899G>A	XP_024303103.1:p.Val967Ile