Canonical Allele Identifier: CA369954740

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1806128A>G (hg19) ; chr8:g.1857962A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857962A>G , CM000670.2:g.1857962A>G	GRCh38
NC_000008.10:g.1806128A>G , CM000670.1:g.1806128A>G	GRCh37
NC_000008.9:g.1793535A>G	NCBI36
NG_008480.1:g.38980A>G , LRG_234:g.38980A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.40A>G MANE Select	ENSP00000340297.3:p.Asn14Asp
ENST00000635773.1:c.499A>G
ENST00000635855.1:c.630A>G	ENSP00000489726.1:p.Lys210=
ENST00000636175.1:c.430A>G
ENST00000349830.7:c.40A>G	ENSP00000340297.3:p.Asn14Asp
ENST00000398564.5:c.112A>G	ENSP00000381571.1:p.Asn38Asp
ENST00000518288.5:c.112A>G	ENSP00000431012.1:p.Asn38Asp
ENST00000520359.5:c.40A>G	ENSP00000427909.1:p.Asn14Asp
NM_001308152.1:c.40A>G	NP_001295081.1:p.Asn14Asp
NM_001308153.1:c.112A>G	NP_001295082.1:p.Asn38Asp
NM_014629.2:c.40A>G , LRG_234t1:c.40A>G	NP_055444.2:p.Asn14Asp
NM_014629.3:c.40A>G	NP_055444.2:p.Asn14Asp
XM_005266041.2:c.40A>G	XP_005266098.1:p.Asn14Asp
XM_011534766.1:c.40A>G	XP_011533068.1:p.Asn14Asp
XM_011534767.1:c.40A>G	XP_011533069.1:p.Asn14Asp
XM_011534768.1:c.40A>G	XP_011533070.1:p.Asn14Asp
XM_011534769.1:c.-6A>G	XP_011533071.1:n.-6A>G
XM_011534770.1:c.40A>G	XP_011533072.1:p.Asn14Asp
XM_005266041.4:c.40A>G	XP_005266098.1:p.Asn14Asp
XM_011534767.2:c.40A>G	XP_011533069.1:p.Asn14Asp
XM_011534770.2:c.40A>G	XP_011533072.1:p.Asn14Asp
XM_017014003.1:c.112A>G	XP_016869492.1:p.Asn38Asp
XM_024447334.1:c.40A>G	XP_024303102.1:p.Asn14Asp
XM_024447335.1:c.124A>G	XP_024303103.1:p.Asn42Asp
NM_014629.4:c.40A>G MANE Select	NP_055444.2:p.Asn14Asp
NM_001308152.2:c.40A>G	NP_001295081.1:p.Asn14Asp
NM_001308153.2:c.112A>G	NP_001295082.1:p.Asn38Asp