Canonical Allele Identifier: CA369954743

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1806129A>G (hg19) ; chr8:g.1857963A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857963A>G , CM000670.2:g.1857963A>G	GRCh38
NC_000008.10:g.1806129A>G , CM000670.1:g.1806129A>G	GRCh37
NC_000008.9:g.1793536A>G	NCBI36
NG_008480.1:g.38981A>G , LRG_234:g.38981A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.41A>G MANE Select	ENSP00000340297.3:p.Asn14Ser
ENST00000635773.1:c.500A>G
ENST00000635855.1:c.631A>G	ENSP00000489726.1:p.Met211Val
ENST00000636175.1:c.431A>G
ENST00000349830.7:c.41A>G	ENSP00000340297.3:p.Asn14Ser
ENST00000398564.5:c.113A>G	ENSP00000381571.1:p.Asn38Ser
ENST00000518288.5:c.113A>G	ENSP00000431012.1:p.Asn38Ser
ENST00000520359.5:c.41A>G	ENSP00000427909.1:p.Asn14Ser
NM_001308152.1:c.41A>G	NP_001295081.1:p.Asn14Ser
NM_001308153.1:c.113A>G	NP_001295082.1:p.Asn38Ser
NM_014629.2:c.41A>G , LRG_234t1:c.41A>G	NP_055444.2:p.Asn14Ser
NM_014629.3:c.41A>G	NP_055444.2:p.Asn14Ser
XM_005266041.2:c.41A>G	XP_005266098.1:p.Asn14Ser
XM_011534766.1:c.41A>G	XP_011533068.1:p.Asn14Ser
XM_011534767.1:c.41A>G	XP_011533069.1:p.Asn14Ser
XM_011534768.1:c.41A>G	XP_011533070.1:p.Asn14Ser
XM_011534769.1:c.-5A>G	XP_011533071.1:n.-5A>G
XM_011534770.1:c.41A>G	XP_011533072.1:p.Asn14Ser
XM_005266041.4:c.41A>G	XP_005266098.1:p.Asn14Ser
XM_011534767.2:c.41A>G	XP_011533069.1:p.Asn14Ser
XM_011534770.2:c.41A>G	XP_011533072.1:p.Asn14Ser
XM_017014003.1:c.113A>G	XP_016869492.1:p.Asn38Ser
XM_024447334.1:c.41A>G	XP_024303102.1:p.Asn14Ser
XM_024447335.1:c.125A>G	XP_024303103.1:p.Asn42Ser
NM_014629.4:c.41A>G MANE Select	NP_055444.2:p.Asn14Ser
NM_001308152.2:c.41A>G	NP_001295081.1:p.Asn14Ser
NM_001308153.2:c.113A>G	NP_001295082.1:p.Asn38Ser