Canonical Allele Identifier: CA1757725069

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857804_1857805delinsCT , CM000670.2:g.1857804_1857805delinsCT	GRCh38
NC_000008.10:g.1805970_1805971delinsCT , CM000670.1:g.1805970_1805971delinsCT	GRCh37
NC_000008.9:g.1793377_1793378delinsCT	NCBI36
NG_008480.1:g.38822_38823delinsCT , LRG_234:g.38822_38823delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-156_38-155delinsCT MANE Select	ENSP00000340297.3:n.38-156_38-155delinsCT
ENST00000635773.1:c.497-156_497-155delinsCT
ENST00000635855.1:c.628-156_628-155delinsCT	ENSP00000489726.1:n.628-156_628-155delinsCT
ENST00000636175.1:c.428-156_428-155delinsCT
ENST00000349830.7:c.38-156_38-155delinsCT	ENSP00000340297.3:n.38-156_38-155delinsCT
ENST00000398564.5:c.110-156_110-155delinsCT	ENSP00000381571.1:n.110-156_110-155delinsCT
ENST00000518288.5:c.110-156_110-155delinsCT	ENSP00000431012.1:n.110-156_110-155delinsCT
ENST00000520359.5:c.38-156_38-155delinsCT	ENSP00000427909.1:n.38-156_38-155delinsCT
NM_001308152.1:c.38-156_38-155delinsCT	NP_001295081.1:n.38-156_38-155delinsCT
NM_001308153.1:c.110-156_110-155delinsCT	NP_001295082.1:n.110-156_110-155delinsCT
NM_014629.2:c.38-156_38-155delinsCT , LRG_234t1:c.38-156_38-155delinsCT	NP_055444.2:n.38-156_38-155delinsCT
NM_014629.3:c.38-156_38-155delinsCT	NP_055444.2:n.38-156_38-155delinsCT
XM_005266041.2:c.38-156_38-155delinsCT	XP_005266098.1:n.38-156_38-155delinsCT
XM_011534766.1:c.38-156_38-155delinsCT	XP_011533068.1:n.38-156_38-155delinsCT
XM_011534767.1:c.38-156_38-155delinsCT	XP_011533069.1:n.38-156_38-155delinsCT
XM_011534768.1:c.38-156_38-155delinsCT	XP_011533070.1:n.38-156_38-155delinsCT
XM_011534769.1:c.-8-156_-8-155delinsCT	XP_011533071.1:n.-8-156_-8-155delinsCT
XM_011534770.1:c.38-156_38-155delinsCT	XP_011533072.1:n.38-156_38-155delinsCT
XM_005266041.4:c.38-156_38-155delinsCT	XP_005266098.1:n.38-156_38-155delinsCT
XM_011534767.2:c.38-156_38-155delinsCT	XP_011533069.1:n.38-156_38-155delinsCT
XM_011534770.2:c.38-156_38-155delinsCT	XP_011533072.1:n.38-156_38-155delinsCT
XM_017014003.1:c.110-156_110-155delinsCT	XP_016869492.1:n.110-156_110-155delinsCT
XM_024447334.1:c.38-156_38-155delinsCT	XP_024303102.1:n.38-156_38-155delinsCT
XM_024447335.1:c.122-156_122-155delinsCT	XP_024303103.1:n.122-156_122-155delinsCT
NM_014629.4:c.38-156_38-155delinsCT MANE Select	NP_055444.2:n.38-156_38-155delinsCT
NM_001308152.2:c.38-156_38-155delinsCT	NP_001295081.1:n.38-156_38-155delinsCT
NM_001308153.2:c.110-156_110-155delinsCT	NP_001295082.1:n.110-156_110-155delinsCT