Canonical Allele Identifier: CA170588672

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1022974188
• gnomAD v2: 8-1806235-C-A
• gnomAD v4: 8-1858069-C-A
• MyVariant Identifiers: chr8:g.1806235C>A (hg19) ; chr8:g.1858069C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1858069C>A , CM000670.2:g.1858069C>A	GRCh38
NC_000008.10:g.1806235C>A , CM000670.1:g.1806235C>A	GRCh37
NC_000008.9:g.1793642C>A	NCBI36
NG_008480.1:g.39087C>A , LRG_234:g.39087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.147C>A MANE Select	ENSP00000340297.3:p.Ala49=
ENST00000635773.1:c.606C>A
ENST00000635855.1:c.*98C>A	ENSP00000489726.1:n.*98C>A
ENST00000636175.1:c.537C>A
ENST00000349830.7:c.147C>A	ENSP00000340297.3:p.Ala49=
ENST00000398564.5:c.219C>A	ENSP00000381571.1:p.Ala73=
ENST00000518288.5:c.219C>A	ENSP00000431012.1:p.Ala73=
ENST00000520359.5:c.147C>A	ENSP00000427909.1:p.Ala49=
NM_001308152.1:c.147C>A	NP_001295081.1:p.Ala49=
NM_001308153.1:c.219C>A	NP_001295082.1:p.Ala73=
NM_014629.2:c.147C>A , LRG_234t1:c.147C>A	NP_055444.2:p.Ala49=
NM_014629.3:c.147C>A	NP_055444.2:p.Ala49=
XM_005266041.2:c.147C>A	XP_005266098.1:p.Ala49=
XM_011534766.1:c.147C>A	XP_011533068.1:p.Ala49=
XM_011534767.1:c.147C>A	XP_011533069.1:p.Ala49=
XM_011534768.1:c.147C>A	XP_011533070.1:p.Ala49=
XM_011534769.1:c.102C>A	XP_011533071.1:p.Ala34=
XM_011534770.1:c.147C>A	XP_011533072.1:p.Ala49=
XM_005266041.4:c.147C>A	XP_005266098.1:p.Ala49=
XM_011534767.2:c.147C>A	XP_011533069.1:p.Ala49=
XM_011534770.2:c.147C>A	XP_011533072.1:p.Ala49=
XM_017014003.1:c.219C>A	XP_016869492.1:p.Ala73=
XM_024447334.1:c.147C>A	XP_024303102.1:p.Ala49=
XM_024447335.1:c.231C>A	XP_024303103.1:p.Ala77=
NM_014629.4:c.147C>A MANE Select	NP_055444.2:p.Ala49=
NM_001308152.2:c.147C>A	NP_001295081.1:p.Ala49=
NM_001308153.2:c.219C>A	NP_001295082.1:p.Ala73=