Canonical Allele Identifier: CA369957299

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900874A>C (hg19) ; chr8:g.1952708A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952708A>C , CM000670.2:g.1952708A>C	GRCh38
NC_000008.10:g.1900874A>C , CM000670.1:g.1900874A>C	GRCh37
NC_000008.9:g.1888281A>C	NCBI36
NG_008480.1:g.133726A>C , LRG_234:g.133726A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3401A>C MANE Select	ENSP00000340297.3:p.His1134Pro
ENST00000635773.1:c.3929A>C
ENST00000635855.1:c.*3355A>C	ENSP00000489726.1:n.*3355A>C
ENST00000349830.7:c.3401A>C	ENSP00000340297.3:p.His1134Pro
ENST00000398564.5:c.3476A>C	ENSP00000381571.1:p.His1159Pro
ENST00000518288.5:c.3473A>C	ENSP00000431012.1:p.His1158Pro
ENST00000520359.5:c.3287A>C	ENSP00000427909.1:p.His1096Pro
ENST00000521927.1:n.238A>C
ENST00000522435.5:c.2333A>C	ENSP00000427768.1:p.His778Pro
ENST00000523596.5:n.493A>C
NM_001308152.1:c.3287A>C	NP_001295081.1:p.His1096Pro
NM_001308153.1:c.3473A>C	NP_001295082.1:p.His1158Pro
NM_014629.2:c.3401A>C , LRG_234t1:c.3401A>C	NP_055444.2:p.His1134Pro
NM_014629.3:c.3401A>C	NP_055444.2:p.His1134Pro
XM_005266041.2:c.3404A>C	XP_005266098.1:p.His1135Pro
XM_011534766.1:c.3317A>C	XP_011533068.1:p.His1106Pro
XM_011534767.1:c.3284A>C	XP_011533069.1:p.His1095Pro
XM_011534768.1:c.3401-4041A>C	XP_011533070.1:n.3401-4041A>C
XM_011534769.1:c.3359A>C	XP_011533071.1:p.His1120Pro
XM_005266041.4:c.3404A>C	XP_005266098.1:p.His1135Pro
XM_011534767.2:c.3284A>C	XP_011533069.1:p.His1095Pro
XM_017014003.1:c.3476A>C	XP_016869492.1:p.His1159Pro
XM_024447334.1:c.3404A>C	XP_024303102.1:p.His1135Pro
XM_024447335.1:c.3488A>C	XP_024303103.1:p.His1163Pro
NM_014629.4:c.3401A>C MANE Select	NP_055444.2:p.His1134Pro
NM_001308152.2:c.3287A>C	NP_001295081.1:p.His1096Pro
NM_001308153.2:c.3473A>C	NP_001295082.1:p.His1158Pro