Canonical Allele Identifier: CA369957310

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900878G>C (hg19) ; chr8:g.1952712G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952712G>C , CM000670.2:g.1952712G>C	GRCh38
NC_000008.10:g.1900878G>C , CM000670.1:g.1900878G>C	GRCh37
NC_000008.9:g.1888285G>C	NCBI36
NG_008480.1:g.133730G>C , LRG_234:g.133730G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3405G>C MANE Select	ENSP00000340297.3:p.Gln1135His
ENST00000635773.1:c.3933G>C
ENST00000635855.1:c.*3359G>C	ENSP00000489726.1:n.*3359G>C
ENST00000349830.7:c.3405G>C	ENSP00000340297.3:p.Gln1135His
ENST00000398564.5:c.3480G>C	ENSP00000381571.1:p.Gln1160His
ENST00000518288.5:c.3477G>C	ENSP00000431012.1:p.Gln1159His
ENST00000520359.5:c.3291G>C	ENSP00000427909.1:p.Gln1097His
ENST00000521927.1:n.242G>C
ENST00000522435.5:c.2337G>C	ENSP00000427768.1:p.Gln779His
ENST00000523596.5:n.497G>C
NM_001308152.1:c.3291G>C	NP_001295081.1:p.Gln1097His
NM_001308153.1:c.3477G>C	NP_001295082.1:p.Gln1159His
NM_014629.2:c.3405G>C , LRG_234t1:c.3405G>C	NP_055444.2:p.Gln1135His
NM_014629.3:c.3405G>C	NP_055444.2:p.Gln1135His
XM_005266041.2:c.3408G>C	XP_005266098.1:p.Gln1136His
XM_011534766.1:c.3321G>C	XP_011533068.1:p.Gln1107His
XM_011534767.1:c.3288G>C	XP_011533069.1:p.Gln1096His
XM_011534768.1:c.3401-4037G>C	XP_011533070.1:n.3401-4037G>C
XM_011534769.1:c.3363G>C	XP_011533071.1:p.Gln1121His
XM_005266041.4:c.3408G>C	XP_005266098.1:p.Gln1136His
XM_011534767.2:c.3288G>C	XP_011533069.1:p.Gln1096His
XM_017014003.1:c.3480G>C	XP_016869492.1:p.Gln1160His
XM_024447334.1:c.3408G>C	XP_024303102.1:p.Gln1136His
XM_024447335.1:c.3492G>C	XP_024303103.1:p.Gln1164His
NM_014629.4:c.3405G>C MANE Select	NP_055444.2:p.Gln1135His
NM_001308152.2:c.3291G>C	NP_001295081.1:p.Gln1097His
NM_001308153.2:c.3477G>C	NP_001295082.1:p.Gln1159His