Canonical Allele Identifier: CA4601364

Gene: ARHGEF10

Linked Data

• ClinVar Variation Id: 2916232
• ClinVar RCV Id: RCV003740325
• dbSNP Id: rs779682833
• ExAC: 8:1900879 C / A
• gnomAD v2: 8-1900879-C-A
• gnomAD v3: 8-1952713-C-A
• gnomAD v4: 8-1952713-C-A
• MyVariant Identifiers: chr8:g.1900879C>A (hg19) ; chr8:g.1952713C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1952713C>A , CM000670.2:g.1952713C>A	GRCh38
NC_000008.10:g.1900879C>A , CM000670.1:g.1900879C>A	GRCh37
NC_000008.9:g.1888286C>A	NCBI36
NG_008480.1:g.133731C>A , LRG_234:g.133731C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.3406C>A MANE Select	ENSP00000340297.3:p.Arg1136=
ENST00000635773.1:c.3934C>A
ENST00000635855.1:c.*3360C>A	ENSP00000489726.1:n.*3360C>A
ENST00000349830.7:c.3406C>A	ENSP00000340297.3:p.Arg1136=
ENST00000398564.5:c.3481C>A	ENSP00000381571.1:p.Arg1161=
ENST00000518288.5:c.3478C>A	ENSP00000431012.1:p.Arg1160=
ENST00000520359.5:c.3292C>A	ENSP00000427909.1:p.Arg1098=
ENST00000521927.1:n.243C>A
ENST00000522435.5:c.2338C>A	ENSP00000427768.1:p.Arg780=
ENST00000523596.5:n.498C>A
NM_001308152.1:c.3292C>A	NP_001295081.1:p.Arg1098=
NM_001308153.1:c.3478C>A	NP_001295082.1:p.Arg1160=
NM_014629.2:c.3406C>A , LRG_234t1:c.3406C>A	NP_055444.2:p.Arg1136=
NM_014629.3:c.3406C>A	NP_055444.2:p.Arg1136=
XM_005266041.2:c.3409C>A	XP_005266098.1:p.Arg1137=
XM_011534766.1:c.3322C>A	XP_011533068.1:p.Arg1108=
XM_011534767.1:c.3289C>A	XP_011533069.1:p.Arg1097=
XM_011534768.1:c.3401-4036C>A	XP_011533070.1:n.3401-4036C>A
XM_011534769.1:c.3364C>A	XP_011533071.1:p.Arg1122=
XM_005266041.4:c.3409C>A	XP_005266098.1:p.Arg1137=
XM_011534767.2:c.3289C>A	XP_011533069.1:p.Arg1097=
XM_017014003.1:c.3481C>A	XP_016869492.1:p.Arg1161=
XM_024447334.1:c.3409C>A	XP_024303102.1:p.Arg1137=
XM_024447335.1:c.3493C>A	XP_024303103.1:p.Arg1165=
NM_014629.4:c.3406C>A MANE Select	NP_055444.2:p.Arg1136=
NM_001308152.2:c.3292C>A	NP_001295081.1:p.Arg1098=
NM_001308153.2:c.3478C>A	NP_001295082.1:p.Arg1160=