Canonical Allele Identifier: CA1109656547
Gene: ARHGEF10 HGNC NCBI

Linked Data

dbSNP Id: rs1805679065

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1857876_1857877insCCTATCTATCTA , CM000670.2:g.1857876_1857877insCCTATCTATCTA GRCh38
NC_000008.10:g.1806042_1806043insCCTATCTATCTA , CM000670.1:g.1806042_1806043insCCTATCTATCTA GRCh37
NC_000008.9:g.1793449_1793450insCCTATCTATCTA NCBI36
NG_008480.1:g.38894_38895insCCTATCTATCTA , LRG_234:g.38894_38895insCCTATCTATCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000349830.8:c.38-84_38-83insCCTATCTATCTA MANE Select ENSP00000340297.3:n.38-84_38-83insCCTATCTATCTA
ENST00000635773.1:c.497-84_497-83insCCTATCTATCTA
ENST00000635855.1:c.628-84_628-83insCCTATCTATCTA ENSP00000489726.1:n.628-84_628-83insCCTATCTATCTA
ENST00000636175.1:c.428-84_428-83insCCTATCTATCTA
ENST00000349830.7:c.38-84_38-83insCCTATCTATCTA ENSP00000340297.3:n.38-84_38-83insCCTATCTATCTA
ENST00000398564.5:c.110-84_110-83insCCTATCTATCTA ENSP00000381571.1:n.110-84_110-83insCCTATCTATCTA
ENST00000518288.5:c.110-84_110-83insCCTATCTATCTA ENSP00000431012.1:n.110-84_110-83insCCTATCTATCTA
ENST00000520359.5:c.38-84_38-83insCCTATCTATCTA ENSP00000427909.1:n.38-84_38-83insCCTATCTATCTA
NM_001308152.1:c.38-84_38-83insCCTATCTATCTA NP_001295081.1:n.38-84_38-83insCCTATCTATCTA
NM_001308153.1:c.110-84_110-83insCCTATCTATCTA NP_001295082.1:n.110-84_110-83insCCTATCTATCTA
NM_014629.2:c.38-84_38-83insCCTATCTATCTA , LRG_234t1:c.38-84_38-83insCCTATCTATCTA NP_055444.2:n.38-84_38-83insCCTATCTATCTA
NM_014629.3:c.38-84_38-83insCCTATCTATCTA NP_055444.2:n.38-84_38-83insCCTATCTATCTA
XM_005266041.2:c.38-84_38-83insCCTATCTATCTA XP_005266098.1:n.38-84_38-83insCCTATCTATCTA
XM_011534766.1:c.38-84_38-83insCCTATCTATCTA XP_011533068.1:n.38-84_38-83insCCTATCTATCTA
XM_011534767.1:c.38-84_38-83insCCTATCTATCTA XP_011533069.1:n.38-84_38-83insCCTATCTATCTA
XM_011534768.1:c.38-84_38-83insCCTATCTATCTA XP_011533070.1:n.38-84_38-83insCCTATCTATCTA
XM_011534769.1:c.-8-84_-8-83insCCTATCTATCTA XP_011533071.1:n.-8-84_-8-83insCCTATCTATCTA
XM_011534770.1:c.38-84_38-83insCCTATCTATCTA XP_011533072.1:n.38-84_38-83insCCTATCTATCTA
XM_005266041.4:c.38-84_38-83insCCTATCTATCTA XP_005266098.1:n.38-84_38-83insCCTATCTATCTA
XM_011534767.2:c.38-84_38-83insCCTATCTATCTA XP_011533069.1:n.38-84_38-83insCCTATCTATCTA
XM_011534770.2:c.38-84_38-83insCCTATCTATCTA XP_011533072.1:n.38-84_38-83insCCTATCTATCTA
XM_017014003.1:c.110-84_110-83insCCTATCTATCTA XP_016869492.1:n.110-84_110-83insCCTATCTATCTA
XM_024447334.1:c.38-84_38-83insCCTATCTATCTA XP_024303102.1:n.38-84_38-83insCCTATCTATCTA
XM_024447335.1:c.122-84_122-83insCCTATCTATCTA XP_024303103.1:n.122-84_122-83insCCTATCTATCTA
NM_014629.4:c.38-84_38-83insCCTATCTATCTA MANE Select NP_055444.2:n.38-84_38-83insCCTATCTATCTA
NM_001308152.2:c.38-84_38-83insCCTATCTATCTA NP_001295081.1:n.38-84_38-83insCCTATCTATCTA
NM_001308153.2:c.110-84_110-83insCCTATCTATCTA NP_001295082.1:n.110-84_110-83insCCTATCTATCTA