Canonical Allele Identifier: CA2838410110

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1870366A>C , CM000670.2:g.1870366A>C	GRCh38
NC_000008.10:g.1818532A>C , CM000670.1:g.1818532A>C	GRCh37
NC_000008.9:g.1805939A>C	NCBI36
NG_008480.1:g.51384A>C , LRG_234:g.51384A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.679+1116A>C MANE Select	ENSP00000340297.3:n.679+1116A>C
ENST00000635773.1:c.1207+1050A>C
ENST00000635855.1:c.*633+1116A>C	ENSP00000489726.1:n.*633+1116A>C
ENST00000349830.7:c.679+1116A>C	ENSP00000340297.3:n.679+1116A>C
ENST00000398560.2:c.64+1116A>C	ENSP00000381568.2:n.64+1116A>C
ENST00000398564.5:c.754+1116A>C	ENSP00000381571.1:n.754+1116A>C
ENST00000518288.5:c.754+1116A>C	ENSP00000431012.1:n.754+1116A>C
ENST00000520359.5:c.682+1116A>C	ENSP00000427909.1:n.682+1116A>C
ENST00000520972.5:n.492+1116A>C
ENST00000522969.1:n.1584A>C
NM_001308152.1:c.682+1116A>C	NP_001295081.1:n.682+1116A>C
NM_001308153.1:c.754+1116A>C	NP_001295082.1:n.754+1116A>C
NM_014629.2:c.679+1116A>C , LRG_234t1:c.679+1116A>C	NP_055444.2:n.679+1116A>C
NM_014629.3:c.679+1116A>C	NP_055444.2:n.679+1116A>C
XM_005266041.2:c.682+1116A>C	XP_005266098.1:n.682+1116A>C
XM_011534766.1:c.682+1116A>C	XP_011533068.1:n.682+1116A>C
XM_011534767.1:c.679+1116A>C	XP_011533069.1:n.679+1116A>C
XM_011534768.1:c.682+1116A>C	XP_011533070.1:n.682+1116A>C
XM_011534769.1:c.637+1116A>C	XP_011533071.1:n.637+1116A>C
XM_011534770.1:c.682+1116A>C	XP_011533072.1:n.682+1116A>C
XM_005266041.4:c.682+1116A>C	XP_005266098.1:n.682+1116A>C
XM_011534767.2:c.679+1116A>C	XP_011533069.1:n.679+1116A>C
XM_011534770.2:c.682+1116A>C	XP_011533072.1:n.682+1116A>C
XM_017014003.1:c.754+1116A>C	XP_016869492.1:n.754+1116A>C
XM_024447334.1:c.682+1116A>C	XP_024303102.1:n.682+1116A>C
XM_024447335.1:c.766+1116A>C	XP_024303103.1:n.766+1116A>C
NM_014629.4:c.679+1116A>C MANE Select	NP_055444.2:n.679+1116A>C
NM_001308152.2:c.682+1116A>C	NP_001295081.1:n.682+1116A>C
NM_001308153.2:c.754+1116A>C	NP_001295082.1:n.754+1116A>C