Canonical Allele Identifier: CA1757785065
Gene: ARHGEF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1952716C= , CM000670.2:g.1952716C= GRCh38
NC_000008.10:g.1900882C= , CM000670.1:g.1900882C= GRCh37
NC_000008.9:g.1888289C= NCBI36
NG_008480.1:g.133734C= , LRG_234:g.133734C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000349830.8:c.3409C= MANE Select ENSP00000340297.3:p.Leu1137=
ENST00000635773.1:c.3937C=
ENST00000635855.1:c.*3363C= ENSP00000489726.1:n.*3363C=
ENST00000349830.7:c.3409C= ENSP00000340297.3:p.Leu1137=
ENST00000398564.5:c.3484C= ENSP00000381571.1:p.Leu1162=
ENST00000518288.5:c.3481C= ENSP00000431012.1:p.Leu1161=
ENST00000520359.5:c.3295C= ENSP00000427909.1:p.Leu1099=
ENST00000521927.1:n.246C=
ENST00000522435.5:c.2341C= ENSP00000427768.1:p.Leu781=
ENST00000523596.5:n.501C=
NM_001308152.1:c.3295C= NP_001295081.1:p.Leu1099=
NM_001308153.1:c.3481C= NP_001295082.1:p.Leu1161=
NM_014629.2:c.3409C= , LRG_234t1:c.3409C= NP_055444.2:p.Leu1137=
NM_014629.3:c.3409C= NP_055444.2:p.Leu1137=
XM_005266041.2:c.3412C= XP_005266098.1:p.Leu1138=
XM_011534766.1:c.3325C= XP_011533068.1:p.Leu1109=
XM_011534767.1:c.3292C= XP_011533069.1:p.Leu1098=
XM_011534768.1:c.3401-4033C= XP_011533070.1:n.3401-4033C=
XM_011534769.1:c.3367C= XP_011533071.1:p.Leu1123=
XM_005266041.4:c.3412C= XP_005266098.1:p.Leu1138=
XM_011534767.2:c.3292C= XP_011533069.1:p.Leu1098=
XM_017014003.1:c.3484C= XP_016869492.1:p.Leu1162=
XM_024447334.1:c.3412C= XP_024303102.1:p.Leu1138=
XM_024447335.1:c.3496C= XP_024303103.1:p.Leu1166=
NM_014629.4:c.3409C= MANE Select NP_055444.2:p.Leu1137=
NM_001308152.2:c.3295C= NP_001295081.1:p.Leu1099=
NM_001308153.2:c.3481C= NP_001295082.1:p.Leu1161=