Canonical Allele Identifier: CA1757725252

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857875_1857891delinsGATCGATCTATCTATCT , CM000670.2:g.1857875_1857891delinsGATCGATCTATCTATCT	GRCh38
NC_000008.10:g.1806041_1806057delinsGATCGATCTATCTATCT , CM000670.1:g.1806041_1806057delinsGATCGATCTATCTATCT	GRCh37
NC_000008.9:g.1793448_1793464delinsGATCGATCTATCTATCT	NCBI36
NG_008480.1:g.38893_38909delinsGATCGATCTATCTATCT , LRG_234:g.38893_38909delinsGATCGATCTATCTATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-85_38-69delinsGATCGATCTATCTATCT MANE Select	ENSP00000340297.3:n.38-85_38-69delinsGATCGATCTATCTATCT
ENST00000635773.1:c.497-85_497-69delinsGATCGATCTATCTATCT
ENST00000635855.1:c.628-85_628-69delinsGATCGATCTATCTATCT	ENSP00000489726.1:n.628-85_628-69delinsGATCGATCTATCTATCT
ENST00000636175.1:c.428-85_428-69delinsGATCGATCTATCTATCT
ENST00000349830.7:c.38-85_38-69delinsGATCGATCTATCTATCT	ENSP00000340297.3:n.38-85_38-69delinsGATCGATCTATCTATCT
ENST00000398564.5:c.110-85_110-69delinsGATCGATCTATCTATCT	ENSP00000381571.1:n.110-85_110-69delinsGATCGATCTATCTATCT
ENST00000518288.5:c.110-85_110-69delinsGATCGATCTATCTATCT	ENSP00000431012.1:n.110-85_110-69delinsGATCGATCTATCTATCT
ENST00000520359.5:c.38-85_38-69delinsGATCGATCTATCTATCT	ENSP00000427909.1:n.38-85_38-69delinsGATCGATCTATCTATCT
NM_001308152.1:c.38-85_38-69delinsGATCGATCTATCTATCT	NP_001295081.1:n.38-85_38-69delinsGATCGATCTATCTATCT
NM_001308153.1:c.110-85_110-69delinsGATCGATCTATCTATCT	NP_001295082.1:n.110-85_110-69delinsGATCGATCTATCTATCT
NM_014629.2:c.38-85_38-69delinsGATCGATCTATCTATCT , LRG_234t1:c.38-85_38-69delinsGATCGATCTATCTATCT	NP_055444.2:n.38-85_38-69delinsGATCGATCTATCTATCT
NM_014629.3:c.38-85_38-69delinsGATCGATCTATCTATCT	NP_055444.2:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_005266041.2:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_005266098.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_011534766.1:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_011533068.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_011534767.1:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_011533069.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_011534768.1:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_011533070.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_011534769.1:c.-8-85_-8-69delinsGATCGATCTATCTATCT	XP_011533071.1:n.-8-85_-8-69delinsGATCGATCTATCTATCT
XM_011534770.1:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_011533072.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_005266041.4:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_005266098.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_011534767.2:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_011533069.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_011534770.2:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_011533072.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_017014003.1:c.110-85_110-69delinsGATCGATCTATCTATCT	XP_016869492.1:n.110-85_110-69delinsGATCGATCTATCTATCT
XM_024447334.1:c.38-85_38-69delinsGATCGATCTATCTATCT	XP_024303102.1:n.38-85_38-69delinsGATCGATCTATCTATCT
XM_024447335.1:c.122-85_122-69delinsGATCGATCTATCTATCT	XP_024303103.1:n.122-85_122-69delinsGATCGATCTATCTATCT
NM_014629.4:c.38-85_38-69delinsGATCGATCTATCTATCT MANE Select	NP_055444.2:n.38-85_38-69delinsGATCGATCTATCTATCT
NM_001308152.2:c.38-85_38-69delinsGATCGATCTATCTATCT	NP_001295081.1:n.38-85_38-69delinsGATCGATCTATCTATCT
NM_001308153.2:c.110-85_110-69delinsGATCGATCTATCTATCT	NP_001295082.1:n.110-85_110-69delinsGATCGATCTATCTATCT