Canonical Allele Identifier: CA369957295

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900871G>C (hg19) ; chr8:g.1952705G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952705G>C , CM000670.2:g.1952705G>C	GRCh38
NC_000008.10:g.1900871G>C , CM000670.1:g.1900871G>C	GRCh37
NC_000008.9:g.1888278G>C	NCBI36
NG_008480.1:g.133723G>C , LRG_234:g.133723G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3398G>C MANE Select	ENSP00000340297.3:p.Gly1133Ala
ENST00000635773.1:c.3926G>C
ENST00000635855.1:c.*3352G>C	ENSP00000489726.1:n.*3352G>C
ENST00000349830.7:c.3398G>C	ENSP00000340297.3:p.Gly1133Ala
ENST00000398564.5:c.3473G>C	ENSP00000381571.1:p.Gly1158Ala
ENST00000518288.5:c.3470G>C	ENSP00000431012.1:p.Gly1157Ala
ENST00000520359.5:c.3284G>C	ENSP00000427909.1:p.Gly1095Ala
ENST00000521927.1:n.235G>C
ENST00000522435.5:c.2330G>C	ENSP00000427768.1:p.Gly777Ala
ENST00000523596.5:n.490G>C
NM_001308152.1:c.3284G>C	NP_001295081.1:p.Gly1095Ala
NM_001308153.1:c.3470G>C	NP_001295082.1:p.Gly1157Ala
NM_014629.2:c.3398G>C , LRG_234t1:c.3398G>C	NP_055444.2:p.Gly1133Ala
NM_014629.3:c.3398G>C	NP_055444.2:p.Gly1133Ala
XM_005266041.2:c.3401G>C	XP_005266098.1:p.Gly1134Ala
XM_011534766.1:c.3314G>C	XP_011533068.1:p.Gly1105Ala
XM_011534767.1:c.3281G>C	XP_011533069.1:p.Gly1094Ala
XM_011534768.1:c.3401-4044G>C	XP_011533070.1:n.3401-4044G>C
XM_011534769.1:c.3356G>C	XP_011533071.1:p.Gly1119Ala
XM_005266041.4:c.3401G>C	XP_005266098.1:p.Gly1134Ala
XM_011534767.2:c.3281G>C	XP_011533069.1:p.Gly1094Ala
XM_017014003.1:c.3473G>C	XP_016869492.1:p.Gly1158Ala
XM_024447334.1:c.3401G>C	XP_024303102.1:p.Gly1134Ala
XM_024447335.1:c.3485G>C	XP_024303103.1:p.Gly1162Ala
NM_014629.4:c.3398G>C MANE Select	NP_055444.2:p.Gly1133Ala
NM_001308152.2:c.3284G>C	NP_001295081.1:p.Gly1095Ala
NM_001308153.2:c.3470G>C	NP_001295082.1:p.Gly1157Ala