Canonical Allele Identifier: CA2685945706

Gene: ARHGEF10

Linked Data

• gnomAD v4: 8-1857953-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857953T>G , CM000670.2:g.1857953T>G	GRCh38
NC_000008.10:g.1806119T>G , CM000670.1:g.1806119T>G	GRCh37
NC_000008.9:g.1793526T>G	NCBI36
NG_008480.1:g.38971T>G , LRG_234:g.38971T>G

Transcript Alleles

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