Canonical Allele Identifier: CA170596399

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1026198444
• gnomAD v2: 8-1900873-C-T
• gnomAD v3: 8-1952707-C-T
• gnomAD v4: 8-1952707-C-T
• MyVariant Identifiers: chr8:g.1900873C>T (hg19) ; chr8:g.1952707C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3400C>T MANE Select	ENSP00000340297.3:p.His1134Tyr
ENST00000635773.1:c.3928C>T
ENST00000635855.1:c.*3354C>T	ENSP00000489726.1:n.*3354C>T
ENST00000349830.7:c.3400C>T	ENSP00000340297.3:p.His1134Tyr
ENST00000398564.5:c.3475C>T	ENSP00000381571.1:p.His1159Tyr
ENST00000518288.5:c.3472C>T	ENSP00000431012.1:p.His1158Tyr
ENST00000520359.5:c.3286C>T	ENSP00000427909.1:p.His1096Tyr
ENST00000521927.1:n.237C>T
ENST00000522435.5:c.2332C>T	ENSP00000427768.1:p.His778Tyr
ENST00000523596.5:n.492C>T
NM_001308152.1:c.3286C>T	NP_001295081.1:p.His1096Tyr
NM_001308153.1:c.3472C>T	NP_001295082.1:p.His1158Tyr
NM_014629.2:c.3400C>T , LRG_234t1:c.3400C>T	NP_055444.2:p.His1134Tyr
NM_014629.3:c.3400C>T	NP_055444.2:p.His1134Tyr
XM_005266041.2:c.3403C>T	XP_005266098.1:p.His1135Tyr
XM_011534766.1:c.3316C>T	XP_011533068.1:p.His1106Tyr
XM_011534767.1:c.3283C>T	XP_011533069.1:p.His1095Tyr
XM_011534768.1:c.3401-4042C>T	XP_011533070.1:n.3401-4042C>T
XM_011534769.1:c.3358C>T	XP_011533071.1:p.His1120Tyr
XM_005266041.4:c.3403C>T	XP_005266098.1:p.His1135Tyr
XM_011534767.2:c.3283C>T	XP_011533069.1:p.His1095Tyr
XM_017014003.1:c.3475C>T	XP_016869492.1:p.His1159Tyr
XM_024447334.1:c.3403C>T	XP_024303102.1:p.His1135Tyr
XM_024447335.1:c.3487C>T	XP_024303103.1:p.His1163Tyr
NM_014629.4:c.3400C>T MANE Select	NP_055444.2:p.His1134Tyr
NM_001308152.2:c.3286C>T	NP_001295081.1:p.His1096Tyr
NM_001308153.2:c.3472C>T	NP_001295082.1:p.His1158Tyr