Canonical Allele Identifier: CA2685945623

Gene: ARHGEF10

Linked Data

• gnomAD v4: 8-1857871-G-GATCTATCTATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857874_1857875insTATCTATCTATC , CM000670.2:g.1857874_1857875insTATCTATCTATC	GRCh38
NC_000008.10:g.1806040_1806041insTATCTATCTATC , CM000670.1:g.1806040_1806041insTATCTATCTATC	GRCh37
NC_000008.9:g.1793447_1793448insTATCTATCTATC	NCBI36
NG_008480.1:g.38892_38893insTATCTATCTATC , LRG_234:g.38892_38893insTATCTATCTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-86_38-85insTATCTATCTATC MANE Select	ENSP00000340297.3:n.38-86_38-85insTATCTATCTATC
ENST00000635773.1:c.497-86_497-85insTATCTATCTATC
ENST00000635855.1:c.628-86_628-85insTATCTATCTATC	ENSP00000489726.1:n.628-86_628-85insTATCTATCTATC
ENST00000636175.1:c.428-86_428-85insTATCTATCTATC
ENST00000349830.7:c.38-86_38-85insTATCTATCTATC	ENSP00000340297.3:n.38-86_38-85insTATCTATCTATC
ENST00000398564.5:c.110-86_110-85insTATCTATCTATC	ENSP00000381571.1:n.110-86_110-85insTATCTATCTATC
ENST00000518288.5:c.110-86_110-85insTATCTATCTATC	ENSP00000431012.1:n.110-86_110-85insTATCTATCTATC
ENST00000520359.5:c.38-86_38-85insTATCTATCTATC	ENSP00000427909.1:n.38-86_38-85insTATCTATCTATC
NM_001308152.1:c.38-86_38-85insTATCTATCTATC	NP_001295081.1:n.38-86_38-85insTATCTATCTATC
NM_001308153.1:c.110-86_110-85insTATCTATCTATC	NP_001295082.1:n.110-86_110-85insTATCTATCTATC
NM_014629.2:c.38-86_38-85insTATCTATCTATC , LRG_234t1:c.38-86_38-85insTATCTATCTATC	NP_055444.2:n.38-86_38-85insTATCTATCTATC
NM_014629.3:c.38-86_38-85insTATCTATCTATC	NP_055444.2:n.38-86_38-85insTATCTATCTATC
XM_005266041.2:c.38-86_38-85insTATCTATCTATC	XP_005266098.1:n.38-86_38-85insTATCTATCTATC
XM_011534766.1:c.38-86_38-85insTATCTATCTATC	XP_011533068.1:n.38-86_38-85insTATCTATCTATC
XM_011534767.1:c.38-86_38-85insTATCTATCTATC	XP_011533069.1:n.38-86_38-85insTATCTATCTATC
XM_011534768.1:c.38-86_38-85insTATCTATCTATC	XP_011533070.1:n.38-86_38-85insTATCTATCTATC
XM_011534769.1:c.-8-86_-8-85insTATCTATCTATC	XP_011533071.1:n.-8-86_-8-85insTATCTATCTATC
XM_011534770.1:c.38-86_38-85insTATCTATCTATC	XP_011533072.1:n.38-86_38-85insTATCTATCTATC
XM_005266041.4:c.38-86_38-85insTATCTATCTATC	XP_005266098.1:n.38-86_38-85insTATCTATCTATC
XM_011534767.2:c.38-86_38-85insTATCTATCTATC	XP_011533069.1:n.38-86_38-85insTATCTATCTATC
XM_011534770.2:c.38-86_38-85insTATCTATCTATC	XP_011533072.1:n.38-86_38-85insTATCTATCTATC
XM_017014003.1:c.110-86_110-85insTATCTATCTATC	XP_016869492.1:n.110-86_110-85insTATCTATCTATC
XM_024447334.1:c.38-86_38-85insTATCTATCTATC	XP_024303102.1:n.38-86_38-85insTATCTATCTATC
XM_024447335.1:c.122-86_122-85insTATCTATCTATC	XP_024303103.1:n.122-86_122-85insTATCTATCTATC
NM_014629.4:c.38-86_38-85insTATCTATCTATC MANE Select	NP_055444.2:n.38-86_38-85insTATCTATCTATC
NM_001308152.2:c.38-86_38-85insTATCTATCTATC	NP_001295081.1:n.38-86_38-85insTATCTATCTATC
NM_001308153.2:c.110-86_110-85insTATCTATCTATC	NP_001295082.1:n.110-86_110-85insTATCTATCTATC