Canonical Allele Identifier: CA369954895
Gene: ARHGEF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1858029G>C , CM000670.2:g.1858029G>C GRCh38
NC_000008.10:g.1806195G>C , CM000670.1:g.1806195G>C GRCh37
NC_000008.9:g.1793602G>C NCBI36
NG_008480.1:g.39047G>C , LRG_234:g.39047G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000349830.8:c.107G>C MANE Select ENSP00000340297.3:p.Gly36Ala
ENST00000635773.1:c.566G>C
ENST00000635855.1:c.*58G>C ENSP00000489726.1:n.*58G>C
ENST00000636175.1:c.497G>C
ENST00000349830.7:c.107G>C ENSP00000340297.3:p.Gly36Ala
ENST00000398564.5:c.179G>C ENSP00000381571.1:p.Gly60Ala
ENST00000518288.5:c.179G>C ENSP00000431012.1:p.Gly60Ala
ENST00000520359.5:c.107G>C ENSP00000427909.1:p.Gly36Ala
NM_001308152.1:c.107G>C NP_001295081.1:p.Gly36Ala
NM_001308153.1:c.179G>C NP_001295082.1:p.Gly60Ala
NM_014629.2:c.107G>C , LRG_234t1:c.107G>C NP_055444.2:p.Gly36Ala
NM_014629.3:c.107G>C NP_055444.2:p.Gly36Ala
XM_005266041.2:c.107G>C XP_005266098.1:p.Gly36Ala
XM_011534766.1:c.107G>C XP_011533068.1:p.Gly36Ala
XM_011534767.1:c.107G>C XP_011533069.1:p.Gly36Ala
XM_011534768.1:c.107G>C XP_011533070.1:p.Gly36Ala
XM_011534769.1:c.62G>C XP_011533071.1:p.Gly21Ala
XM_011534770.1:c.107G>C XP_011533072.1:p.Gly36Ala
XM_005266041.4:c.107G>C XP_005266098.1:p.Gly36Ala
XM_011534767.2:c.107G>C XP_011533069.1:p.Gly36Ala
XM_011534770.2:c.107G>C XP_011533072.1:p.Gly36Ala
XM_017014003.1:c.179G>C XP_016869492.1:p.Gly60Ala
XM_024447334.1:c.107G>C XP_024303102.1:p.Gly36Ala
XM_024447335.1:c.191G>C XP_024303103.1:p.Gly64Ala
NM_014629.4:c.107G>C MANE Select NP_055444.2:p.Gly36Ala
NM_001308152.2:c.107G>C NP_001295081.1:p.Gly36Ala
NM_001308153.2:c.179G>C NP_001295082.1:p.Gly60Ala