Canonical Allele Identifier: CA1757725479
Gene: ARHGEF10 HGNC NCBI

Linked Data

dbSNP Id: rs1480282816

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1857909_1857910insGTAT , CM000670.2:g.1857909_1857910insGTAT GRCh38
NC_000008.10:g.1806075_1806076insGTAT , CM000670.1:g.1806075_1806076insGTAT GRCh37
NC_000008.9:g.1793482_1793483insGTAT NCBI36
NG_008480.1:g.38927_38928insGTAT , LRG_234:g.38927_38928insGTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000349830.8:c.38-51_38-50insGTAT MANE Select ENSP00000340297.3:n.38-51_38-50insGTAT
ENST00000635773.1:c.497-51_497-50insGTAT
ENST00000635855.1:c.628-51_628-50insGTAT ENSP00000489726.1:n.628-51_628-50insGTAT
ENST00000636175.1:c.428-51_428-50insGTAT
ENST00000349830.7:c.38-51_38-50insGTAT ENSP00000340297.3:n.38-51_38-50insGTAT
ENST00000398564.5:c.110-51_110-50insGTAT ENSP00000381571.1:n.110-51_110-50insGTAT
ENST00000518288.5:c.110-51_110-50insGTAT ENSP00000431012.1:n.110-51_110-50insGTAT
ENST00000520359.5:c.38-51_38-50insGTAT ENSP00000427909.1:n.38-51_38-50insGTAT
NM_001308152.1:c.38-51_38-50insGTAT NP_001295081.1:n.38-51_38-50insGTAT
NM_001308153.1:c.110-51_110-50insGTAT NP_001295082.1:n.110-51_110-50insGTAT
NM_014629.2:c.38-51_38-50insGTAT , LRG_234t1:c.38-51_38-50insGTAT NP_055444.2:n.38-51_38-50insGTAT
NM_014629.3:c.38-51_38-50insGTAT NP_055444.2:n.38-51_38-50insGTAT
XM_005266041.2:c.38-51_38-50insGTAT XP_005266098.1:n.38-51_38-50insGTAT
XM_011534766.1:c.38-51_38-50insGTAT XP_011533068.1:n.38-51_38-50insGTAT
XM_011534767.1:c.38-51_38-50insGTAT XP_011533069.1:n.38-51_38-50insGTAT
XM_011534768.1:c.38-51_38-50insGTAT XP_011533070.1:n.38-51_38-50insGTAT
XM_011534769.1:c.-8-51_-8-50insGTAT XP_011533071.1:n.-8-51_-8-50insGTAT
XM_011534770.1:c.38-51_38-50insGTAT XP_011533072.1:n.38-51_38-50insGTAT
XM_005266041.4:c.38-51_38-50insGTAT XP_005266098.1:n.38-51_38-50insGTAT
XM_011534767.2:c.38-51_38-50insGTAT XP_011533069.1:n.38-51_38-50insGTAT
XM_011534770.2:c.38-51_38-50insGTAT XP_011533072.1:n.38-51_38-50insGTAT
XM_017014003.1:c.110-51_110-50insGTAT XP_016869492.1:n.110-51_110-50insGTAT
XM_024447334.1:c.38-51_38-50insGTAT XP_024303102.1:n.38-51_38-50insGTAT
XM_024447335.1:c.122-51_122-50insGTAT XP_024303103.1:n.122-51_122-50insGTAT
NM_014629.4:c.38-51_38-50insGTAT MANE Select NP_055444.2:n.38-51_38-50insGTAT
NM_001308152.2:c.38-51_38-50insGTAT NP_001295081.1:n.38-51_38-50insGTAT
NM_001308153.2:c.110-51_110-50insGTAT NP_001295082.1:n.110-51_110-50insGTAT