Canonical Allele Identifier: CA369955017

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1806257G>A (hg19) ; chr8:g.1858091G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858091G>A , CM000670.2:g.1858091G>A	GRCh38
NC_000008.10:g.1806257G>A , CM000670.1:g.1806257G>A	GRCh37
NC_000008.9:g.1793664G>A	NCBI36
NG_008480.1:g.39109G>A , LRG_234:g.39109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.169G>A MANE Select	ENSP00000340297.3:p.Ala57Thr
ENST00000635773.1:c.628G>A
ENST00000635855.1:c.*120G>A	ENSP00000489726.1:n.*120G>A
ENST00000636175.1:c.559G>A
ENST00000349830.7:c.169G>A	ENSP00000340297.3:p.Ala57Thr
ENST00000398564.5:c.241G>A	ENSP00000381571.1:p.Ala81Thr
ENST00000518288.5:c.241G>A	ENSP00000431012.1:p.Ala81Thr
ENST00000520359.5:c.169G>A	ENSP00000427909.1:p.Ala57Thr
NM_001308152.1:c.169G>A	NP_001295081.1:p.Ala57Thr
NM_001308153.1:c.241G>A	NP_001295082.1:p.Ala81Thr
NM_014629.2:c.169G>A , LRG_234t1:c.169G>A	NP_055444.2:p.Ala57Thr
NM_014629.3:c.169G>A	NP_055444.2:p.Ala57Thr
XM_005266041.2:c.169G>A	XP_005266098.1:p.Ala57Thr
XM_011534766.1:c.169G>A	XP_011533068.1:p.Ala57Thr
XM_011534767.1:c.169G>A	XP_011533069.1:p.Ala57Thr
XM_011534768.1:c.169G>A	XP_011533070.1:p.Ala57Thr
XM_011534769.1:c.124G>A	XP_011533071.1:p.Ala42Thr
XM_011534770.1:c.169G>A	XP_011533072.1:p.Ala57Thr
XM_005266041.4:c.169G>A	XP_005266098.1:p.Ala57Thr
XM_011534767.2:c.169G>A	XP_011533069.1:p.Ala57Thr
XM_011534770.2:c.169G>A	XP_011533072.1:p.Ala57Thr
XM_017014003.1:c.241G>A	XP_016869492.1:p.Ala81Thr
XM_024447334.1:c.169G>A	XP_024303102.1:p.Ala57Thr
XM_024447335.1:c.253G>A	XP_024303103.1:p.Ala85Thr
NM_014629.4:c.169G>A MANE Select	NP_055444.2:p.Ala57Thr
NM_001308152.2:c.169G>A	NP_001295081.1:p.Ala57Thr
NM_001308153.2:c.241G>A	NP_001295082.1:p.Ala81Thr