Canonical Allele Identifier: CA369954801

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1806153A>C (hg19) ; chr8:g.1857987A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857987A>C , CM000670.2:g.1857987A>C	GRCh38
NC_000008.10:g.1806153A>C , CM000670.1:g.1806153A>C	GRCh37
NC_000008.9:g.1793560A>C	NCBI36
NG_008480.1:g.39005A>C , LRG_234:g.39005A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.65A>C MANE Select	ENSP00000340297.3:p.Asn22Thr
ENST00000635773.1:c.524A>C
ENST00000635855.1:c.*16A>C	ENSP00000489726.1:n.*16A>C
ENST00000636175.1:c.455A>C
ENST00000349830.7:c.65A>C	ENSP00000340297.3:p.Asn22Thr
ENST00000398564.5:c.137A>C	ENSP00000381571.1:p.Asn46Thr
ENST00000518288.5:c.137A>C	ENSP00000431012.1:p.Asn46Thr
ENST00000520359.5:c.65A>C	ENSP00000427909.1:p.Asn22Thr
NM_001308152.1:c.65A>C	NP_001295081.1:p.Asn22Thr
NM_001308153.1:c.137A>C	NP_001295082.1:p.Asn46Thr
NM_014629.2:c.65A>C , LRG_234t1:c.65A>C	NP_055444.2:p.Asn22Thr
NM_014629.3:c.65A>C	NP_055444.2:p.Asn22Thr
XM_005266041.2:c.65A>C	XP_005266098.1:p.Asn22Thr
XM_011534766.1:c.65A>C	XP_011533068.1:p.Asn22Thr
XM_011534767.1:c.65A>C	XP_011533069.1:p.Asn22Thr
XM_011534768.1:c.65A>C	XP_011533070.1:p.Asn22Thr
XM_011534769.1:c.20A>C	XP_011533071.1:p.Asn7Thr
XM_011534770.1:c.65A>C	XP_011533072.1:p.Asn22Thr
XM_005266041.4:c.65A>C	XP_005266098.1:p.Asn22Thr
XM_011534767.2:c.65A>C	XP_011533069.1:p.Asn22Thr
XM_011534770.2:c.65A>C	XP_011533072.1:p.Asn22Thr
XM_017014003.1:c.137A>C	XP_016869492.1:p.Asn46Thr
XM_024447334.1:c.65A>C	XP_024303102.1:p.Asn22Thr
XM_024447335.1:c.149A>C	XP_024303103.1:p.Asn50Thr
NM_014629.4:c.65A>C MANE Select	NP_055444.2:p.Asn22Thr
NM_001308152.2:c.65A>C	NP_001295081.1:p.Asn22Thr
NM_001308153.2:c.137A>C	NP_001295082.1:p.Asn46Thr