Canonical Allele Identifier: CA2590771590

Gene: ARHGEF10

Linked Data

• gnomAD v3: 8-1858143-A-AGTACCCAGGTGG
• gnomAD v4: 8-1858143-A-AGTACCCAGGTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858145_1858146insACCCAGGTGGGT , CM000670.2:g.1858145_1858146insACCCAGGTGGGT	GRCh38
NC_000008.10:g.1806311_1806312insACCCAGGTGGGT , CM000670.1:g.1806311_1806312insACCCAGGTGGGT	GRCh37
NC_000008.9:g.1793718_1793719insACCCAGGTGGGT	NCBI36
NG_008480.1:g.39163_39164insACCCAGGTGGGT , LRG_234:g.39163_39164insACCCAGGTGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.193+30_193+31insACCCAGGTGGGT MANE Select	ENSP00000340297.3:n.193+30_193+31insACCCAGGTGGGT
ENST00000635773.1:c.652+30_652+31insACCCAGGTGGGT
ENST00000635855.1:c.*144+30_*144+31insACCCAGGTGGGT	ENSP00000489726.1:n.*144+30_*144+31insACCCAGGTGGGT
ENST00000636175.1:c.583+30_583+31insACCCAGGTGGGT
ENST00000349830.7:c.193+30_193+31insACCCAGGTGGGT	ENSP00000340297.3:n.193+30_193+31insACCCAGGTGGGT
ENST00000398564.5:c.265+30_265+31insACCCAGGTGGGT	ENSP00000381571.1:n.265+30_265+31insACCCAGGTGGGT
ENST00000518288.5:c.265+30_265+31insACCCAGGTGGGT	ENSP00000431012.1:n.265+30_265+31insACCCAGGTGGGT
ENST00000520359.5:c.193+30_193+31insACCCAGGTGGGT	ENSP00000427909.1:n.193+30_193+31insACCCAGGTGGGT
NM_001308152.1:c.193+30_193+31insACCCAGGTGGGT	NP_001295081.1:n.193+30_193+31insACCCAGGTGGGT
NM_001308153.1:c.265+30_265+31insACCCAGGTGGGT	NP_001295082.1:n.265+30_265+31insACCCAGGTGGGT
NM_014629.2:c.193+30_193+31insACCCAGGTGGGT , LRG_234t1:c.193+30_193+31insACCCAGGTGGGT	NP_055444.2:n.193+30_193+31insACCCAGGTGGGT
NM_014629.3:c.193+30_193+31insACCCAGGTGGGT	NP_055444.2:n.193+30_193+31insACCCAGGTGGGT
XM_005266041.2:c.193+30_193+31insACCCAGGTGGGT	XP_005266098.1:n.193+30_193+31insACCCAGGTGGGT
XM_011534766.1:c.193+30_193+31insACCCAGGTGGGT	XP_011533068.1:n.193+30_193+31insACCCAGGTGGGT
XM_011534767.1:c.193+30_193+31insACCCAGGTGGGT	XP_011533069.1:n.193+30_193+31insACCCAGGTGGGT
XM_011534768.1:c.193+30_193+31insACCCAGGTGGGT	XP_011533070.1:n.193+30_193+31insACCCAGGTGGGT
XM_011534769.1:c.148+30_148+31insACCCAGGTGGGT	XP_011533071.1:n.148+30_148+31insACCCAGGTGGGT
XM_011534770.1:c.193+30_193+31insACCCAGGTGGGT	XP_011533072.1:n.193+30_193+31insACCCAGGTGGGT
XM_005266041.4:c.193+30_193+31insACCCAGGTGGGT	XP_005266098.1:n.193+30_193+31insACCCAGGTGGGT
XM_011534767.2:c.193+30_193+31insACCCAGGTGGGT	XP_011533069.1:n.193+30_193+31insACCCAGGTGGGT
XM_011534770.2:c.193+30_193+31insACCCAGGTGGGT	XP_011533072.1:n.193+30_193+31insACCCAGGTGGGT
XM_017014003.1:c.265+30_265+31insACCCAGGTGGGT	XP_016869492.1:n.265+30_265+31insACCCAGGTGGGT
XM_024447334.1:c.193+30_193+31insACCCAGGTGGGT	XP_024303102.1:n.193+30_193+31insACCCAGGTGGGT
XM_024447335.1:c.277+30_277+31insACCCAGGTGGGT	XP_024303103.1:n.277+30_277+31insACCCAGGTGGGT
NM_014629.4:c.193+30_193+31insACCCAGGTGGGT MANE Select	NP_055444.2:n.193+30_193+31insACCCAGGTGGGT
NM_001308152.2:c.193+30_193+31insACCCAGGTGGGT	NP_001295081.1:n.193+30_193+31insACCCAGGTGGGT
NM_001308153.2:c.265+30_265+31insACCCAGGTGGGT	NP_001295082.1:n.265+30_265+31insACCCAGGTGGGT