Canonical Allele Identifier: CA369957313

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900880G>C (hg19) ; chr8:g.1952714G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952714G>C , CM000670.2:g.1952714G>C	GRCh38
NC_000008.10:g.1900880G>C , CM000670.1:g.1900880G>C	GRCh37
NC_000008.9:g.1888287G>C	NCBI36
NG_008480.1:g.133732G>C , LRG_234:g.133732G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3407G>C MANE Select	ENSP00000340297.3:p.Arg1136Pro
ENST00000635773.1:c.3935G>C
ENST00000635855.1:c.*3361G>C	ENSP00000489726.1:n.*3361G>C
ENST00000349830.7:c.3407G>C	ENSP00000340297.3:p.Arg1136Pro
ENST00000398564.5:c.3482G>C	ENSP00000381571.1:p.Arg1161Pro
ENST00000518288.5:c.3479G>C	ENSP00000431012.1:p.Arg1160Pro
ENST00000520359.5:c.3293G>C	ENSP00000427909.1:p.Arg1098Pro
ENST00000521927.1:n.244G>C
ENST00000522435.5:c.2339G>C	ENSP00000427768.1:p.Arg780Pro
ENST00000523596.5:n.499G>C
NM_001308152.1:c.3293G>C	NP_001295081.1:p.Arg1098Pro
NM_001308153.1:c.3479G>C	NP_001295082.1:p.Arg1160Pro
NM_014629.2:c.3407G>C , LRG_234t1:c.3407G>C	NP_055444.2:p.Arg1136Pro
NM_014629.3:c.3407G>C	NP_055444.2:p.Arg1136Pro
XM_005266041.2:c.3410G>C	XP_005266098.1:p.Arg1137Pro
XM_011534766.1:c.3323G>C	XP_011533068.1:p.Arg1108Pro
XM_011534767.1:c.3290G>C	XP_011533069.1:p.Arg1097Pro
XM_011534768.1:c.3401-4035G>C	XP_011533070.1:n.3401-4035G>C
XM_011534769.1:c.3365G>C	XP_011533071.1:p.Arg1122Pro
XM_005266041.4:c.3410G>C	XP_005266098.1:p.Arg1137Pro
XM_011534767.2:c.3290G>C	XP_011533069.1:p.Arg1097Pro
XM_017014003.1:c.3482G>C	XP_016869492.1:p.Arg1161Pro
XM_024447334.1:c.3410G>C	XP_024303102.1:p.Arg1137Pro
XM_024447335.1:c.3494G>C	XP_024303103.1:p.Arg1165Pro
NM_014629.4:c.3407G>C MANE Select	NP_055444.2:p.Arg1136Pro
NM_001308152.2:c.3293G>C	NP_001295081.1:p.Arg1098Pro
NM_001308153.2:c.3479G>C	NP_001295082.1:p.Arg1160Pro