Canonical Allele Identifier: CA849456660

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1250244489
• gnomAD v4: 8-1857886-C-CTATT
• MyVariant Identifiers: chr8:g.1806052_1806053insTATT (hg19) ; chr8:g.1857886_1857887insTATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857889_1857890insTTAT , CM000670.2:g.1857889_1857890insTTAT	GRCh38
NC_000008.10:g.1806055_1806056insTTAT , CM000670.1:g.1806055_1806056insTTAT	GRCh37
NC_000008.9:g.1793462_1793463insTTAT	NCBI36
NG_008480.1:g.38907_38908insTTAT , LRG_234:g.38907_38908insTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-71_38-70insTTAT MANE Select	ENSP00000340297.3:n.38-71_38-70insTTAT
ENST00000635773.1:c.497-71_497-70insTTAT
ENST00000635855.1:c.628-71_628-70insTTAT	ENSP00000489726.1:n.628-71_628-70insTTAT
ENST00000636175.1:c.428-71_428-70insTTAT
ENST00000349830.7:c.38-71_38-70insTTAT	ENSP00000340297.3:n.38-71_38-70insTTAT
ENST00000398564.5:c.110-71_110-70insTTAT	ENSP00000381571.1:n.110-71_110-70insTTAT
ENST00000518288.5:c.110-71_110-70insTTAT	ENSP00000431012.1:n.110-71_110-70insTTAT
ENST00000520359.5:c.38-71_38-70insTTAT	ENSP00000427909.1:n.38-71_38-70insTTAT
NM_001308152.1:c.38-71_38-70insTTAT	NP_001295081.1:n.38-71_38-70insTTAT
NM_001308153.1:c.110-71_110-70insTTAT	NP_001295082.1:n.110-71_110-70insTTAT
NM_014629.2:c.38-71_38-70insTTAT , LRG_234t1:c.38-71_38-70insTTAT	NP_055444.2:n.38-71_38-70insTTAT
NM_014629.3:c.38-71_38-70insTTAT	NP_055444.2:n.38-71_38-70insTTAT
XM_005266041.2:c.38-71_38-70insTTAT	XP_005266098.1:n.38-71_38-70insTTAT
XM_011534766.1:c.38-71_38-70insTTAT	XP_011533068.1:n.38-71_38-70insTTAT
XM_011534767.1:c.38-71_38-70insTTAT	XP_011533069.1:n.38-71_38-70insTTAT
XM_011534768.1:c.38-71_38-70insTTAT	XP_011533070.1:n.38-71_38-70insTTAT
XM_011534769.1:c.-8-71_-8-70insTTAT	XP_011533071.1:n.-8-71_-8-70insTTAT
XM_011534770.1:c.38-71_38-70insTTAT	XP_011533072.1:n.38-71_38-70insTTAT
XM_005266041.4:c.38-71_38-70insTTAT	XP_005266098.1:n.38-71_38-70insTTAT
XM_011534767.2:c.38-71_38-70insTTAT	XP_011533069.1:n.38-71_38-70insTTAT
XM_011534770.2:c.38-71_38-70insTTAT	XP_011533072.1:n.38-71_38-70insTTAT
XM_017014003.1:c.110-71_110-70insTTAT	XP_016869492.1:n.110-71_110-70insTTAT
XM_024447334.1:c.38-71_38-70insTTAT	XP_024303102.1:n.38-71_38-70insTTAT
XM_024447335.1:c.122-71_122-70insTTAT	XP_024303103.1:n.122-71_122-70insTTAT
NM_014629.4:c.38-71_38-70insTTAT MANE Select	NP_055444.2:n.38-71_38-70insTTAT
NM_001308152.2:c.38-71_38-70insTTAT	NP_001295081.1:n.38-71_38-70insTTAT
NM_001308153.2:c.110-71_110-70insTTAT	NP_001295082.1:n.110-71_110-70insTTAT