Canonical Allele Identifier: CA2685945858
Gene: ARHGEF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1858163_1858164del , CM000670.2:g.1858163_1858164del GRCh38
NC_000008.10:g.1806329_1806330del , CM000670.1:g.1806329_1806330del GRCh37
NC_000008.9:g.1793736_1793737del NCBI36
NG_008480.1:g.39181_39182del , LRG_234:g.39181_39182del

Transcript Alleles

HGVS Amino-acid Change
ENST00000349830.8:c.193+48_193+49del MANE Select ENSP00000340297.3:n.193+48_193+49del
ENST00000635773.1:c.652+48_652+49del
ENST00000635855.1:c.*144+48_*144+49del ENSP00000489726.1:n.*144+48_*144+49del
ENST00000636175.1:c.583+48_583+49del
ENST00000349830.7:c.193+48_193+49del ENSP00000340297.3:n.193+48_193+49del
ENST00000398564.5:c.265+48_265+49del ENSP00000381571.1:n.265+48_265+49del
ENST00000518288.5:c.265+48_265+49del ENSP00000431012.1:n.265+48_265+49del
ENST00000520359.5:c.193+48_193+49del ENSP00000427909.1:n.193+48_193+49del
NM_001308152.1:c.193+48_193+49del NP_001295081.1:n.193+48_193+49del
NM_001308153.1:c.265+48_265+49del NP_001295082.1:n.265+48_265+49del
NM_014629.2:c.193+48_193+49del , LRG_234t1:c.193+48_193+49del NP_055444.2:n.193+48_193+49del
NM_014629.3:c.193+48_193+49del NP_055444.2:n.193+48_193+49del
XM_005266041.2:c.193+48_193+49del XP_005266098.1:n.193+48_193+49del
XM_011534766.1:c.193+48_193+49del XP_011533068.1:n.193+48_193+49del
XM_011534767.1:c.193+48_193+49del XP_011533069.1:n.193+48_193+49del
XM_011534768.1:c.193+48_193+49del XP_011533070.1:n.193+48_193+49del
XM_011534769.1:c.148+48_148+49del XP_011533071.1:n.148+48_148+49del
XM_011534770.1:c.193+48_193+49del XP_011533072.1:n.193+48_193+49del
XM_005266041.4:c.193+48_193+49del XP_005266098.1:n.193+48_193+49del
XM_011534767.2:c.193+48_193+49del XP_011533069.1:n.193+48_193+49del
XM_011534770.2:c.193+48_193+49del XP_011533072.1:n.193+48_193+49del
XM_017014003.1:c.265+48_265+49del XP_016869492.1:n.265+48_265+49del
XM_024447334.1:c.193+48_193+49del XP_024303102.1:n.193+48_193+49del
XM_024447335.1:c.277+48_277+49del XP_024303103.1:n.277+48_277+49del
NM_014629.4:c.193+48_193+49del MANE Select NP_055444.2:n.193+48_193+49del
NM_001308152.2:c.193+48_193+49del NP_001295081.1:n.193+48_193+49del
NM_001308153.2:c.265+48_265+49del NP_001295082.1:n.265+48_265+49del