Canonical Allele Identifier: CA369957303

Gene: ARHGEF10

Linked Data

• MyVariant Identifiers: chr8:g.1900875C>G (hg19) ; chr8:g.1952709C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952709C>G , CM000670.2:g.1952709C>G	GRCh38
NC_000008.10:g.1900875C>G , CM000670.1:g.1900875C>G	GRCh37
NC_000008.9:g.1888282C>G	NCBI36
NG_008480.1:g.133727C>G , LRG_234:g.133727C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3402C>G MANE Select	ENSP00000340297.3:p.His1134Gln
ENST00000635773.1:c.3930C>G
ENST00000635855.1:c.*3356C>G	ENSP00000489726.1:n.*3356C>G
ENST00000349830.7:c.3402C>G	ENSP00000340297.3:p.His1134Gln
ENST00000398564.5:c.3477C>G	ENSP00000381571.1:p.His1159Gln
ENST00000518288.5:c.3474C>G	ENSP00000431012.1:p.His1158Gln
ENST00000520359.5:c.3288C>G	ENSP00000427909.1:p.His1096Gln
ENST00000521927.1:n.239C>G
ENST00000522435.5:c.2334C>G	ENSP00000427768.1:p.His778Gln
ENST00000523596.5:n.494C>G
NM_001308152.1:c.3288C>G	NP_001295081.1:p.His1096Gln
NM_001308153.1:c.3474C>G	NP_001295082.1:p.His1158Gln
NM_014629.2:c.3402C>G , LRG_234t1:c.3402C>G	NP_055444.2:p.His1134Gln
NM_014629.3:c.3402C>G	NP_055444.2:p.His1134Gln
XM_005266041.2:c.3405C>G	XP_005266098.1:p.His1135Gln
XM_011534766.1:c.3318C>G	XP_011533068.1:p.His1106Gln
XM_011534767.1:c.3285C>G	XP_011533069.1:p.His1095Gln
XM_011534768.1:c.3401-4040C>G	XP_011533070.1:n.3401-4040C>G
XM_011534769.1:c.3360C>G	XP_011533071.1:p.His1120Gln
XM_005266041.4:c.3405C>G	XP_005266098.1:p.His1135Gln
XM_011534767.2:c.3285C>G	XP_011533069.1:p.His1095Gln
XM_017014003.1:c.3477C>G	XP_016869492.1:p.His1159Gln
XM_024447334.1:c.3405C>G	XP_024303102.1:p.His1135Gln
XM_024447335.1:c.3489C>G	XP_024303103.1:p.His1163Gln
NM_014629.4:c.3402C>G MANE Select	NP_055444.2:p.His1134Gln
NM_001308152.2:c.3288C>G	NP_001295081.1:p.His1096Gln
NM_001308153.2:c.3474C>G	NP_001295082.1:p.His1158Gln