Canonical Allele Identifier: CA459050204

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900878G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952712G>A , CM000670.2:g.1952712G>A	GRCh38
NC_000008.10:g.1900878G>A , CM000670.1:g.1900878G>A	GRCh37
NC_000008.9:g.1888285G>A	NCBI36
NG_008480.1:g.133730G>A , LRG_234:g.133730G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.3405G>A MANE Select	ENSP00000340297.3:p.Gln1135=
ENST00000635773.1:c.3933G>A
ENST00000635855.1:c.*3359G>A	ENSP00000489726.1:n.*3359G>A
ENST00000349830.7:c.3405G>A	ENSP00000340297.3:p.Gln1135=
ENST00000398564.5:c.3480G>A	ENSP00000381571.1:p.Gln1160=
ENST00000518288.5:c.3477G>A	ENSP00000431012.1:p.Gln1159=
ENST00000520359.5:c.3291G>A	ENSP00000427909.1:p.Gln1097=
ENST00000521927.1:n.242G>A
ENST00000522435.5:c.2337G>A	ENSP00000427768.1:p.Gln779=
ENST00000523596.5:n.497G>A
NM_001308152.1:c.3291G>A	NP_001295081.1:p.Gln1097=
NM_001308153.1:c.3477G>A	NP_001295082.1:p.Gln1159=
NM_014629.2:c.3405G>A , LRG_234t1:c.3405G>A	NP_055444.2:p.Gln1135=
NM_014629.3:c.3405G>A	NP_055444.2:p.Gln1135=
XM_005266041.2:c.3408G>A	XP_005266098.1:p.Gln1136=
XM_011534766.1:c.3321G>A	XP_011533068.1:p.Gln1107=
XM_011534767.1:c.3288G>A	XP_011533069.1:p.Gln1096=
XM_011534768.1:c.3401-4037G>A	XP_011533070.1:n.3401-4037G>A
XM_011534769.1:c.3363G>A	XP_011533071.1:p.Gln1121=
XM_005266041.4:c.3408G>A	XP_005266098.1:p.Gln1136=
XM_011534767.2:c.3288G>A	XP_011533069.1:p.Gln1096=
XM_017014003.1:c.3480G>A	XP_016869492.1:p.Gln1160=
XM_024447334.1:c.3408G>A	XP_024303102.1:p.Gln1136=
XM_024447335.1:c.3492G>A	XP_024303103.1:p.Gln1164=
NM_014629.4:c.3405G>A MANE Select	NP_055444.2:p.Gln1135=
NM_001308152.2:c.3291G>A	NP_001295081.1:p.Gln1097=
NM_001308153.2:c.3477G>A	NP_001295082.1:p.Gln1159=