Canonical Allele Identifier: CA579305007

Gene: ARHGEF10

Linked Data

• dbSNP Id: rs1343718628
• gnomAD v2: 8-1806053-T-TATCG
• gnomAD v3: 8-1857887-T-TATCG
• gnomAD v4: 8-1857887-T-TATCG
• MyVariant Identifiers: chr8:g.1806053_1806054insATCG (hg19) ; chr8:g.1857887_1857888insATCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1857890_1857891insGATC , CM000670.2:g.1857890_1857891insGATC	GRCh38
NC_000008.10:g.1806056_1806057insGATC , CM000670.1:g.1806056_1806057insGATC	GRCh37
NC_000008.9:g.1793463_1793464insGATC	NCBI36
NG_008480.1:g.38908_38909insGATC , LRG_234:g.38908_38909insGATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349830.8:c.38-70_38-69insGATC MANE Select	ENSP00000340297.3:n.38-70_38-69insGATC
ENST00000635773.1:c.497-70_497-69insGATC
ENST00000635855.1:c.628-70_628-69insGATC	ENSP00000489726.1:n.628-70_628-69insGATC
ENST00000636175.1:c.428-70_428-69insGATC
ENST00000349830.7:c.38-70_38-69insGATC	ENSP00000340297.3:n.38-70_38-69insGATC
ENST00000398564.5:c.110-70_110-69insGATC	ENSP00000381571.1:n.110-70_110-69insGATC
ENST00000518288.5:c.110-70_110-69insGATC	ENSP00000431012.1:n.110-70_110-69insGATC
ENST00000520359.5:c.38-70_38-69insGATC	ENSP00000427909.1:n.38-70_38-69insGATC
NM_001308152.1:c.38-70_38-69insGATC	NP_001295081.1:n.38-70_38-69insGATC
NM_001308153.1:c.110-70_110-69insGATC	NP_001295082.1:n.110-70_110-69insGATC
NM_014629.2:c.38-70_38-69insGATC , LRG_234t1:c.38-70_38-69insGATC	NP_055444.2:n.38-70_38-69insGATC
NM_014629.3:c.38-70_38-69insGATC	NP_055444.2:n.38-70_38-69insGATC
XM_005266041.2:c.38-70_38-69insGATC	XP_005266098.1:n.38-70_38-69insGATC
XM_011534766.1:c.38-70_38-69insGATC	XP_011533068.1:n.38-70_38-69insGATC
XM_011534767.1:c.38-70_38-69insGATC	XP_011533069.1:n.38-70_38-69insGATC
XM_011534768.1:c.38-70_38-69insGATC	XP_011533070.1:n.38-70_38-69insGATC
XM_011534769.1:c.-8-70_-8-69insGATC	XP_011533071.1:n.-8-70_-8-69insGATC
XM_011534770.1:c.38-70_38-69insGATC	XP_011533072.1:n.38-70_38-69insGATC
XM_005266041.4:c.38-70_38-69insGATC	XP_005266098.1:n.38-70_38-69insGATC
XM_011534767.2:c.38-70_38-69insGATC	XP_011533069.1:n.38-70_38-69insGATC
XM_011534770.2:c.38-70_38-69insGATC	XP_011533072.1:n.38-70_38-69insGATC
XM_017014003.1:c.110-70_110-69insGATC	XP_016869492.1:n.110-70_110-69insGATC
XM_024447334.1:c.38-70_38-69insGATC	XP_024303102.1:n.38-70_38-69insGATC
XM_024447335.1:c.122-70_122-69insGATC	XP_024303103.1:n.122-70_122-69insGATC
NM_014629.4:c.38-70_38-69insGATC MANE Select	NP_055444.2:n.38-70_38-69insGATC
NM_001308152.2:c.38-70_38-69insGATC	NP_001295081.1:n.38-70_38-69insGATC
NM_001308153.2:c.110-70_110-69insGATC	NP_001295082.1:n.110-70_110-69insGATC