Canonical Allele Identifier: CA369957312

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900879C>G (hg19) ; chr8:g.1952713C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952713C>G , CM000670.2:g.1952713C>G	GRCh38
NC_000008.10:g.1900879C>G , CM000670.1:g.1900879C>G	GRCh37
NC_000008.9:g.1888286C>G	NCBI36
NG_008480.1:g.133731C>G , LRG_234:g.133731C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.3406C>G MANE Select	ENSP00000340297.3:p.Arg1136Gly
ENST00000635773.1:c.3934C>G
ENST00000635855.1:c.*3360C>G	ENSP00000489726.1:n.*3360C>G
ENST00000349830.7:c.3406C>G	ENSP00000340297.3:p.Arg1136Gly
ENST00000398564.5:c.3481C>G	ENSP00000381571.1:p.Arg1161Gly
ENST00000518288.5:c.3478C>G	ENSP00000431012.1:p.Arg1160Gly
ENST00000520359.5:c.3292C>G	ENSP00000427909.1:p.Arg1098Gly
ENST00000521927.1:n.243C>G
ENST00000522435.5:c.2338C>G	ENSP00000427768.1:p.Arg780Gly
ENST00000523596.5:n.498C>G
NM_001308152.1:c.3292C>G	NP_001295081.1:p.Arg1098Gly
NM_001308153.1:c.3478C>G	NP_001295082.1:p.Arg1160Gly
NM_014629.2:c.3406C>G , LRG_234t1:c.3406C>G	NP_055444.2:p.Arg1136Gly
NM_014629.3:c.3406C>G	NP_055444.2:p.Arg1136Gly
XM_005266041.2:c.3409C>G	XP_005266098.1:p.Arg1137Gly
XM_011534766.1:c.3322C>G	XP_011533068.1:p.Arg1108Gly
XM_011534767.1:c.3289C>G	XP_011533069.1:p.Arg1097Gly
XM_011534768.1:c.3401-4036C>G	XP_011533070.1:n.3401-4036C>G
XM_011534769.1:c.3364C>G	XP_011533071.1:p.Arg1122Gly
XM_005266041.4:c.3409C>G	XP_005266098.1:p.Arg1137Gly
XM_011534767.2:c.3289C>G	XP_011533069.1:p.Arg1097Gly
XM_017014003.1:c.3481C>G	XP_016869492.1:p.Arg1161Gly
XM_024447334.1:c.3409C>G	XP_024303102.1:p.Arg1137Gly
XM_024447335.1:c.3493C>G	XP_024303103.1:p.Arg1165Gly
NM_014629.4:c.3406C>G MANE Select	NP_055444.2:p.Arg1136Gly
NM_001308152.2:c.3292C>G	NP_001295081.1:p.Arg1098Gly
NM_001308153.2:c.3478C>G	NP_001295082.1:p.Arg1160Gly