Canonical Allele Identifier: CA1757725653

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857964T= , CM000670.2:g.1857964T=	GRCh38
NC_000008.10:g.1806130T= , CM000670.1:g.1806130T=	GRCh37
NC_000008.9:g.1793537T=	NCBI36
NG_008480.1:g.38982T= , LRG_234:g.38982T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.42T= MANE Select	ENSP00000340297.3:p.Asn14=
ENST00000635773.1:c.501T=
ENST00000635855.1:c.632T=	ENSP00000489726.1:p.Met211=
ENST00000636175.1:c.432T=
ENST00000349830.7:c.42T=	ENSP00000340297.3:p.Asn14=
ENST00000398564.5:c.114T=	ENSP00000381571.1:p.Asn38=
ENST00000518288.5:c.114T=	ENSP00000431012.1:p.Asn38=
ENST00000520359.5:c.42T=	ENSP00000427909.1:p.Asn14=
NM_001308152.1:c.42T=	NP_001295081.1:p.Asn14=
NM_001308153.1:c.114T=	NP_001295082.1:p.Asn38=
NM_014629.2:c.42T= , LRG_234t1:c.42T=	NP_055444.2:p.Asn14=
NM_014629.3:c.42T=	NP_055444.2:p.Asn14=
XM_005266041.2:c.42T=	XP_005266098.1:p.Asn14=
XM_011534766.1:c.42T=	XP_011533068.1:p.Asn14=
XM_011534767.1:c.42T=	XP_011533069.1:p.Asn14=
XM_011534768.1:c.42T=	XP_011533070.1:p.Asn14=
XM_011534769.1:c.-4T=	XP_011533071.1:n.-4T=
XM_011534770.1:c.42T=	XP_011533072.1:p.Asn14=
XM_005266041.4:c.42T=	XP_005266098.1:p.Asn14=
XM_011534767.2:c.42T=	XP_011533069.1:p.Asn14=
XM_011534770.2:c.42T=	XP_011533072.1:p.Asn14=
XM_017014003.1:c.114T=	XP_016869492.1:p.Asn38=
XM_024447334.1:c.42T=	XP_024303102.1:p.Asn14=
XM_024447335.1:c.126T=	XP_024303103.1:p.Asn42=
NM_014629.4:c.42T= MANE Select	NP_055444.2:p.Asn14=
NM_001308152.2:c.42T=	NP_001295081.1:p.Asn14=
NM_001308153.2:c.114T=	NP_001295082.1:p.Asn38=