Canonical Allele Identifier: CA1757724950

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857731_1857733delinsCTG , CM000670.2:g.1857731_1857733delinsCTG	GRCh38
NC_000008.10:g.1805897_1805899delinsCTG , CM000670.1:g.1805897_1805899delinsCTG	GRCh37
NC_000008.9:g.1793304_1793306delinsCTG	NCBI36
NG_008480.1:g.38749_38751delinsCTG , LRG_234:g.38749_38751delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-229_38-227delinsCTG MANE Select	ENSP00000340297.3:n.38-229_38-227delinsCTG
ENST00000635773.1:c.497-229_497-227delinsCTG
ENST00000635855.1:c.628-229_628-227delinsCTG	ENSP00000489726.1:n.628-229_628-227delinsCTG
ENST00000636175.1:c.428-229_428-227delinsCTG
ENST00000349830.7:c.38-229_38-227delinsCTG	ENSP00000340297.3:n.38-229_38-227delinsCTG
ENST00000398564.5:c.110-229_110-227delinsCTG	ENSP00000381571.1:n.110-229_110-227delinsCTG
ENST00000518288.5:c.110-229_110-227delinsCTG	ENSP00000431012.1:n.110-229_110-227delinsCTG
ENST00000520359.5:c.38-229_38-227delinsCTG	ENSP00000427909.1:n.38-229_38-227delinsCTG
NM_001308152.1:c.38-229_38-227delinsCTG	NP_001295081.1:n.38-229_38-227delinsCTG
NM_001308153.1:c.110-229_110-227delinsCTG	NP_001295082.1:n.110-229_110-227delinsCTG
NM_014629.2:c.38-229_38-227delinsCTG , LRG_234t1:c.38-229_38-227delinsCTG	NP_055444.2:n.38-229_38-227delinsCTG
NM_014629.3:c.38-229_38-227delinsCTG	NP_055444.2:n.38-229_38-227delinsCTG
XM_005266041.2:c.38-229_38-227delinsCTG	XP_005266098.1:n.38-229_38-227delinsCTG
XM_011534766.1:c.38-229_38-227delinsCTG	XP_011533068.1:n.38-229_38-227delinsCTG
XM_011534767.1:c.38-229_38-227delinsCTG	XP_011533069.1:n.38-229_38-227delinsCTG
XM_011534768.1:c.38-229_38-227delinsCTG	XP_011533070.1:n.38-229_38-227delinsCTG
XM_011534769.1:c.-8-229_-8-227delinsCTG	XP_011533071.1:n.-8-229_-8-227delinsCTG
XM_011534770.1:c.38-229_38-227delinsCTG	XP_011533072.1:n.38-229_38-227delinsCTG
XM_005266041.4:c.38-229_38-227delinsCTG	XP_005266098.1:n.38-229_38-227delinsCTG
XM_011534767.2:c.38-229_38-227delinsCTG	XP_011533069.1:n.38-229_38-227delinsCTG
XM_011534770.2:c.38-229_38-227delinsCTG	XP_011533072.1:n.38-229_38-227delinsCTG
XM_017014003.1:c.110-229_110-227delinsCTG	XP_016869492.1:n.110-229_110-227delinsCTG
XM_024447334.1:c.38-229_38-227delinsCTG	XP_024303102.1:n.38-229_38-227delinsCTG
XM_024447335.1:c.122-229_122-227delinsCTG	XP_024303103.1:n.122-229_122-227delinsCTG
NM_014629.4:c.38-229_38-227delinsCTG MANE Select	NP_055444.2:n.38-229_38-227delinsCTG
NM_001308152.2:c.38-229_38-227delinsCTG	NP_001295081.1:n.38-229_38-227delinsCTG
NM_001308153.2:c.110-229_110-227delinsCTG	NP_001295082.1:n.110-229_110-227delinsCTG