Canonical Allele Identifier: CA1757784882

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952548_1952549delinsGC , CM000670.2:g.1952548_1952549delinsGC	GRCh38
NC_000008.10:g.1900714_1900715delinsGC , CM000670.1:g.1900714_1900715delinsGC	GRCh37
NC_000008.9:g.1888121_1888122delinsGC	NCBI36
NG_008480.1:g.133566_133567delinsGC , LRG_234:g.133566_133567delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.3398-157_3398-156delinsGC MANE Select	ENSP00000340297.3:n.3398-157_3398-156delinsGC
ENST00000635773.1:c.3926-157_3926-156delinsGC
ENST00000635855.1:c.*3352-157_*3352-156delinsGC	ENSP00000489726.1:n.*3352-157_*3352-156delinsGC
ENST00000349830.7:c.3398-157_3398-156delinsGC	ENSP00000340297.3:n.3398-157_3398-156delinsGC
ENST00000398564.5:c.3473-157_3473-156delinsGC	ENSP00000381571.1:n.3473-157_3473-156delinsGC
ENST00000518288.5:c.3470-157_3470-156delinsGC	ENSP00000431012.1:n.3470-157_3470-156delinsGC
ENST00000520359.5:c.3284-157_3284-156delinsGC	ENSP00000427909.1:n.3284-157_3284-156delinsGC
ENST00000521927.1:n.235-157_235-156delinsGC
ENST00000522435.5:c.2330-157_2330-156delinsGC	ENSP00000427768.1:n.2330-157_2330-156delinsGC
ENST00000523596.5:n.490-157_490-156delinsGC
NM_001308152.1:c.3284-157_3284-156delinsGC	NP_001295081.1:n.3284-157_3284-156delinsGC
NM_001308153.1:c.3470-157_3470-156delinsGC	NP_001295082.1:n.3470-157_3470-156delinsGC
NM_014629.2:c.3398-157_3398-156delinsGC , LRG_234t1:c.3398-157_3398-156delinsGC	NP_055444.2:n.3398-157_3398-156delinsGC
NM_014629.3:c.3398-157_3398-156delinsGC	NP_055444.2:n.3398-157_3398-156delinsGC
XM_005266041.2:c.3401-157_3401-156delinsGC	XP_005266098.1:n.3401-157_3401-156delinsGC
XM_011534766.1:c.3314-157_3314-156delinsGC	XP_011533068.1:n.3314-157_3314-156delinsGC
XM_011534767.1:c.3281-157_3281-156delinsGC	XP_011533069.1:n.3281-157_3281-156delinsGC
XM_011534768.1:c.3401-4201_3401-4200delinsGC	XP_011533070.1:n.3401-4201_3401-4200delinsGC
XM_011534769.1:c.3356-157_3356-156delinsGC	XP_011533071.1:n.3356-157_3356-156delinsGC
XM_005266041.4:c.3401-157_3401-156delinsGC	XP_005266098.1:n.3401-157_3401-156delinsGC
XM_011534767.2:c.3281-157_3281-156delinsGC	XP_011533069.1:n.3281-157_3281-156delinsGC
XM_017014003.1:c.3473-157_3473-156delinsGC	XP_016869492.1:n.3473-157_3473-156delinsGC
XM_024447334.1:c.3401-157_3401-156delinsGC	XP_024303102.1:n.3401-157_3401-156delinsGC
XM_024447335.1:c.3485-157_3485-156delinsGC	XP_024303103.1:n.3485-157_3485-156delinsGC
NM_014629.4:c.3398-157_3398-156delinsGC MANE Select	NP_055444.2:n.3398-157_3398-156delinsGC
NM_001308152.2:c.3284-157_3284-156delinsGC	NP_001295081.1:n.3284-157_3284-156delinsGC
NM_001308153.2:c.3470-157_3470-156delinsGC	NP_001295082.1:n.3470-157_3470-156delinsGC