Canonical Allele Identifier: CA579304941

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1333768391
• gnomAD v2: 8-1806037-G-GATCT
• gnomAD v3: 8-1857871-G-GATCT
• gnomAD v4: 8-1857871-G-GATCT
• MyVariant Identifiers: chr8:g.1806041_1806049delinsTATCGATCGATCT (hg19) ; chr8:g.1806037_1806038insATCT (hg19) ; chr8:g.1857875_1857883delinsTATCGATCGATCT (hg38) ; chr8:g.1857871_1857872insATCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857874_1857875insTATC , CM000670.2:g.1857874_1857875insTATC	GRCh38
NC_000008.10:g.1806040_1806041insTATC , CM000670.1:g.1806040_1806041insTATC	GRCh37
NC_000008.9:g.1793447_1793448insTATC	NCBI36
NG_008480.1:g.38892_38893insTATC , LRG_234:g.38892_38893insTATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000349830.8:c.38-86_38-85insTATC MANE Select	ENSP00000340297.3:n.38-86_38-85insTATC
ENST00000635773.1:c.497-86_497-85insTATC
ENST00000635855.1:c.628-86_628-85insTATC	ENSP00000489726.1:n.628-86_628-85insTATC
ENST00000636175.1:c.428-86_428-85insTATC
ENST00000349830.7:c.38-86_38-85insTATC	ENSP00000340297.3:n.38-86_38-85insTATC
ENST00000398564.5:c.110-86_110-85insTATC	ENSP00000381571.1:n.110-86_110-85insTATC
ENST00000518288.5:c.110-86_110-85insTATC	ENSP00000431012.1:n.110-86_110-85insTATC
ENST00000520359.5:c.38-86_38-85insTATC	ENSP00000427909.1:n.38-86_38-85insTATC
NM_001308152.1:c.38-86_38-85insTATC	NP_001295081.1:n.38-86_38-85insTATC
NM_001308153.1:c.110-86_110-85insTATC	NP_001295082.1:n.110-86_110-85insTATC
NM_014629.2:c.38-86_38-85insTATC , LRG_234t1:c.38-86_38-85insTATC	NP_055444.2:n.38-86_38-85insTATC
NM_014629.3:c.38-86_38-85insTATC	NP_055444.2:n.38-86_38-85insTATC
XM_005266041.2:c.38-86_38-85insTATC	XP_005266098.1:n.38-86_38-85insTATC
XM_011534766.1:c.38-86_38-85insTATC	XP_011533068.1:n.38-86_38-85insTATC
XM_011534767.1:c.38-86_38-85insTATC	XP_011533069.1:n.38-86_38-85insTATC
XM_011534768.1:c.38-86_38-85insTATC	XP_011533070.1:n.38-86_38-85insTATC
XM_011534769.1:c.-8-86_-8-85insTATC	XP_011533071.1:n.-8-86_-8-85insTATC
XM_011534770.1:c.38-86_38-85insTATC	XP_011533072.1:n.38-86_38-85insTATC
XM_005266041.4:c.38-86_38-85insTATC	XP_005266098.1:n.38-86_38-85insTATC
XM_011534767.2:c.38-86_38-85insTATC	XP_011533069.1:n.38-86_38-85insTATC
XM_011534770.2:c.38-86_38-85insTATC	XP_011533072.1:n.38-86_38-85insTATC
XM_017014003.1:c.110-86_110-85insTATC	XP_016869492.1:n.110-86_110-85insTATC
XM_024447334.1:c.38-86_38-85insTATC	XP_024303102.1:n.38-86_38-85insTATC
XM_024447335.1:c.122-86_122-85insTATC	XP_024303103.1:n.122-86_122-85insTATC
NM_014629.4:c.38-86_38-85insTATC MANE Select	NP_055444.2:n.38-86_38-85insTATC
NM_001308152.2:c.38-86_38-85insTATC	NP_001295081.1:n.38-86_38-85insTATC
NM_001308153.2:c.110-86_110-85insTATC	NP_001295082.1:n.110-86_110-85insTATC