Canonical Allele Identifier: CA1757784847

Gene: ARHGEF10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952510G= , CM000670.2:g.1952510G=	GRCh38
NC_000008.10:g.1900676G= , CM000670.1:g.1900676G=	GRCh37
NC_000008.9:g.1888083G=	NCBI36
NG_008480.1:g.133528G= , LRG_234:g.133528G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.3398-195G= MANE Select	ENSP00000340297.3:n.3398-195G=
ENST00000635773.1:c.3926-195G=
ENST00000635855.1:c.*3352-195G=	ENSP00000489726.1:n.*3352-195G=
ENST00000349830.7:c.3398-195G=	ENSP00000340297.3:n.3398-195G=
ENST00000398564.5:c.3473-195G=	ENSP00000381571.1:n.3473-195G=
ENST00000518288.5:c.3470-195G=	ENSP00000431012.1:n.3470-195G=
ENST00000520359.5:c.3284-195G=	ENSP00000427909.1:n.3284-195G=
ENST00000521927.1:n.235-195G=
ENST00000522435.5:c.2330-195G=	ENSP00000427768.1:n.2330-195G=
ENST00000523596.5:n.490-195G=
NM_001308152.1:c.3284-195G=	NP_001295081.1:n.3284-195G=
NM_001308153.1:c.3470-195G=	NP_001295082.1:n.3470-195G=
NM_014629.2:c.3398-195G= , LRG_234t1:c.3398-195G=	NP_055444.2:n.3398-195G=
NM_014629.3:c.3398-195G=	NP_055444.2:n.3398-195G=
XM_005266041.2:c.3401-195G=	XP_005266098.1:n.3401-195G=
XM_011534766.1:c.3314-195G=	XP_011533068.1:n.3314-195G=
XM_011534767.1:c.3281-195G=	XP_011533069.1:n.3281-195G=
XM_011534768.1:c.3401-4239G=	XP_011533070.1:n.3401-4239G=
XM_011534769.1:c.3356-195G=	XP_011533071.1:n.3356-195G=
XM_005266041.4:c.3401-195G=	XP_005266098.1:n.3401-195G=
XM_011534767.2:c.3281-195G=	XP_011533069.1:n.3281-195G=
XM_017014003.1:c.3473-195G=	XP_016869492.1:n.3473-195G=
XM_024447334.1:c.3401-195G=	XP_024303102.1:n.3401-195G=
XM_024447335.1:c.3485-195G=	XP_024303103.1:n.3485-195G=
NM_014629.4:c.3398-195G= MANE Select	NP_055444.2:n.3398-195G=
NM_001308152.2:c.3284-195G=	NP_001295081.1:n.3284-195G=
NM_001308153.2:c.3470-195G=	NP_001295082.1:n.3470-195G=