Canonical Allele Identifier: CA2716047732
Gene: ARHGEF10 HGNC NCBI

Linked Data

dbSNP Id: rs1264861539

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1857887_1857888insCTCT , CM000670.2:g.1857887_1857888insCTCT GRCh38
NC_000008.10:g.1806053_1806054insCTCT , CM000670.1:g.1806053_1806054insCTCT GRCh37
NC_000008.9:g.1793460_1793461insCTCT NCBI36
NG_008480.1:g.38905_38906insCTCT , LRG_234:g.38905_38906insCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000349830.8:c.38-73_38-72insCTCT MANE Select ENSP00000340297.3:n.38-73_38-72insCTCT
ENST00000635773.1:c.497-73_497-72insCTCT
ENST00000635855.1:c.628-73_628-72insCTCT ENSP00000489726.1:n.628-73_628-72insCTCT
ENST00000636175.1:c.428-73_428-72insCTCT
ENST00000349830.7:c.38-73_38-72insCTCT ENSP00000340297.3:n.38-73_38-72insCTCT
ENST00000398564.5:c.110-73_110-72insCTCT ENSP00000381571.1:n.110-73_110-72insCTCT
ENST00000518288.5:c.110-73_110-72insCTCT ENSP00000431012.1:n.110-73_110-72insCTCT
ENST00000520359.5:c.38-73_38-72insCTCT ENSP00000427909.1:n.38-73_38-72insCTCT
NM_001308152.1:c.38-73_38-72insCTCT NP_001295081.1:n.38-73_38-72insCTCT
NM_001308153.1:c.110-73_110-72insCTCT NP_001295082.1:n.110-73_110-72insCTCT
NM_014629.2:c.38-73_38-72insCTCT , LRG_234t1:c.38-73_38-72insCTCT NP_055444.2:n.38-73_38-72insCTCT
NM_014629.3:c.38-73_38-72insCTCT NP_055444.2:n.38-73_38-72insCTCT
XM_005266041.2:c.38-73_38-72insCTCT XP_005266098.1:n.38-73_38-72insCTCT
XM_011534766.1:c.38-73_38-72insCTCT XP_011533068.1:n.38-73_38-72insCTCT
XM_011534767.1:c.38-73_38-72insCTCT XP_011533069.1:n.38-73_38-72insCTCT
XM_011534768.1:c.38-73_38-72insCTCT XP_011533070.1:n.38-73_38-72insCTCT
XM_011534769.1:c.-8-73_-8-72insCTCT XP_011533071.1:n.-8-73_-8-72insCTCT
XM_011534770.1:c.38-73_38-72insCTCT XP_011533072.1:n.38-73_38-72insCTCT
XM_005266041.4:c.38-73_38-72insCTCT XP_005266098.1:n.38-73_38-72insCTCT
XM_011534767.2:c.38-73_38-72insCTCT XP_011533069.1:n.38-73_38-72insCTCT
XM_011534770.2:c.38-73_38-72insCTCT XP_011533072.1:n.38-73_38-72insCTCT
XM_017014003.1:c.110-73_110-72insCTCT XP_016869492.1:n.110-73_110-72insCTCT
XM_024447334.1:c.38-73_38-72insCTCT XP_024303102.1:n.38-73_38-72insCTCT
XM_024447335.1:c.122-73_122-72insCTCT XP_024303103.1:n.122-73_122-72insCTCT
NM_014629.4:c.38-73_38-72insCTCT MANE Select NP_055444.2:n.38-73_38-72insCTCT
NM_001308152.2:c.38-73_38-72insCTCT NP_001295081.1:n.38-73_38-72insCTCT
NM_001308153.2:c.110-73_110-72insCTCT NP_001295082.1:n.110-73_110-72insCTCT