Canonical Allele Identifier: CA369957298

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1026198444
• MyVariant Identifiers: chr8:g.1900873C>A (hg19) ; chr8:g.1952707C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952707C>A , CM000670.2:g.1952707C>A	GRCh38
NC_000008.10:g.1900873C>A , CM000670.1:g.1900873C>A	GRCh37
NC_000008.9:g.1888280C>A	NCBI36
NG_008480.1:g.133725C>A , LRG_234:g.133725C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3400C>A MANE Select	ENSP00000340297.3:p.His1134Asn
ENST00000635773.1:c.3928C>A
ENST00000635855.1:c.*3354C>A	ENSP00000489726.1:n.*3354C>A
ENST00000349830.7:c.3400C>A	ENSP00000340297.3:p.His1134Asn
ENST00000398564.5:c.3475C>A	ENSP00000381571.1:p.His1159Asn
ENST00000518288.5:c.3472C>A	ENSP00000431012.1:p.His1158Asn
ENST00000520359.5:c.3286C>A	ENSP00000427909.1:p.His1096Asn
ENST00000521927.1:n.237C>A
ENST00000522435.5:c.2332C>A	ENSP00000427768.1:p.His778Asn
ENST00000523596.5:n.492C>A
NM_001308152.1:c.3286C>A	NP_001295081.1:p.His1096Asn
NM_001308153.1:c.3472C>A	NP_001295082.1:p.His1158Asn
NM_014629.2:c.3400C>A , LRG_234t1:c.3400C>A	NP_055444.2:p.His1134Asn
NM_014629.3:c.3400C>A	NP_055444.2:p.His1134Asn
XM_005266041.2:c.3403C>A	XP_005266098.1:p.His1135Asn
XM_011534766.1:c.3316C>A	XP_011533068.1:p.His1106Asn
XM_011534767.1:c.3283C>A	XP_011533069.1:p.His1095Asn
XM_011534768.1:c.3401-4042C>A	XP_011533070.1:n.3401-4042C>A
XM_011534769.1:c.3358C>A	XP_011533071.1:p.His1120Asn
XM_005266041.4:c.3403C>A	XP_005266098.1:p.His1135Asn
XM_011534767.2:c.3283C>A	XP_011533069.1:p.His1095Asn
XM_017014003.1:c.3475C>A	XP_016869492.1:p.His1159Asn
XM_024447334.1:c.3403C>A	XP_024303102.1:p.His1135Asn
XM_024447335.1:c.3487C>A	XP_024303103.1:p.His1163Asn
NM_014629.4:c.3400C>A MANE Select	NP_055444.2:p.His1134Asn
NM_001308152.2:c.3286C>A	NP_001295081.1:p.His1096Asn
NM_001308153.2:c.3472C>A	NP_001295082.1:p.His1158Asn