Canonical Allele Identifier: CA2685945692

Gene: ARHGEF10

Linked Data

• gnomAD v4: 8-1857927-T-TATCTATCTCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857927_1857928insATCTATCTCTCC , CM000670.2:g.1857927_1857928insATCTATCTCTCC	GRCh38
NC_000008.10:g.1806093_1806094insATCTATCTCTCC , CM000670.1:g.1806093_1806094insATCTATCTCTCC	GRCh37
NC_000008.9:g.1793500_1793501insATCTATCTCTCC	NCBI36
NG_008480.1:g.38945_38946insATCTATCTCTCC , LRG_234:g.38945_38946insATCTATCTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-33_38-32insATCTATCTCTCC MANE Select	ENSP00000340297.3:n.38-33_38-32insATCTATCTCTCC
ENST00000635773.1:c.497-33_497-32insATCTATCTCTCC
ENST00000635855.1:c.628-33_628-32insATCTATCTCTCC	ENSP00000489726.1:n.628-33_628-32insATCTATCTCTCC
ENST00000636175.1:c.428-33_428-32insATCTATCTCTCC
ENST00000349830.7:c.38-33_38-32insATCTATCTCTCC	ENSP00000340297.3:n.38-33_38-32insATCTATCTCTCC
ENST00000398564.5:c.110-33_110-32insATCTATCTCTCC	ENSP00000381571.1:n.110-33_110-32insATCTATCTCTCC
ENST00000518288.5:c.110-33_110-32insATCTATCTCTCC	ENSP00000431012.1:n.110-33_110-32insATCTATCTCTCC
ENST00000520359.5:c.38-33_38-32insATCTATCTCTCC	ENSP00000427909.1:n.38-33_38-32insATCTATCTCTCC
NM_001308152.1:c.38-33_38-32insATCTATCTCTCC	NP_001295081.1:n.38-33_38-32insATCTATCTCTCC
NM_001308153.1:c.110-33_110-32insATCTATCTCTCC	NP_001295082.1:n.110-33_110-32insATCTATCTCTCC
NM_014629.2:c.38-33_38-32insATCTATCTCTCC , LRG_234t1:c.38-33_38-32insATCTATCTCTCC	NP_055444.2:n.38-33_38-32insATCTATCTCTCC
NM_014629.3:c.38-33_38-32insATCTATCTCTCC	NP_055444.2:n.38-33_38-32insATCTATCTCTCC
XM_005266041.2:c.38-33_38-32insATCTATCTCTCC	XP_005266098.1:n.38-33_38-32insATCTATCTCTCC
XM_011534766.1:c.38-33_38-32insATCTATCTCTCC	XP_011533068.1:n.38-33_38-32insATCTATCTCTCC
XM_011534767.1:c.38-33_38-32insATCTATCTCTCC	XP_011533069.1:n.38-33_38-32insATCTATCTCTCC
XM_011534768.1:c.38-33_38-32insATCTATCTCTCC	XP_011533070.1:n.38-33_38-32insATCTATCTCTCC
XM_011534769.1:c.-8-33_-8-32insATCTATCTCTCC	XP_011533071.1:n.-8-33_-8-32insATCTATCTCTCC
XM_011534770.1:c.38-33_38-32insATCTATCTCTCC	XP_011533072.1:n.38-33_38-32insATCTATCTCTCC
XM_005266041.4:c.38-33_38-32insATCTATCTCTCC	XP_005266098.1:n.38-33_38-32insATCTATCTCTCC
XM_011534767.2:c.38-33_38-32insATCTATCTCTCC	XP_011533069.1:n.38-33_38-32insATCTATCTCTCC
XM_011534770.2:c.38-33_38-32insATCTATCTCTCC	XP_011533072.1:n.38-33_38-32insATCTATCTCTCC
XM_017014003.1:c.110-33_110-32insATCTATCTCTCC	XP_016869492.1:n.110-33_110-32insATCTATCTCTCC
XM_024447334.1:c.38-33_38-32insATCTATCTCTCC	XP_024303102.1:n.38-33_38-32insATCTATCTCTCC
XM_024447335.1:c.122-33_122-32insATCTATCTCTCC	XP_024303103.1:n.122-33_122-32insATCTATCTCTCC
NM_014629.4:c.38-33_38-32insATCTATCTCTCC MANE Select	NP_055444.2:n.38-33_38-32insATCTATCTCTCC
NM_001308152.2:c.38-33_38-32insATCTATCTCTCC	NP_001295081.1:n.38-33_38-32insATCTATCTCTCC
NM_001308153.2:c.110-33_110-32insATCTATCTCTCC	NP_001295082.1:n.110-33_110-32insATCTATCTCTCC