Canonical Allele Identifier: CA1757784936
Gene: ARHGEF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1952614A= , CM000670.2:g.1952614A= GRCh38
NC_000008.10:g.1900780A= , CM000670.1:g.1900780A= GRCh37
NC_000008.9:g.1888187A= NCBI36
NG_008480.1:g.133632A= , LRG_234:g.133632A=

Transcript Alleles

HGVS Amino-acid change
ENST00000349830.8:c.3398-91A= MANE Select ENSP00000340297.3:n.3398-91A=
ENST00000635773.1:c.3926-91A=
ENST00000635855.1:c.*3352-91A= ENSP00000489726.1:n.*3352-91A=
ENST00000349830.7:c.3398-91A= ENSP00000340297.3:n.3398-91A=
ENST00000398564.5:c.3473-91A= ENSP00000381571.1:n.3473-91A=
ENST00000518288.5:c.3470-91A= ENSP00000431012.1:n.3470-91A=
ENST00000520359.5:c.3284-91A= ENSP00000427909.1:n.3284-91A=
ENST00000521927.1:n.235-91A=
ENST00000522435.5:c.2330-91A= ENSP00000427768.1:n.2330-91A=
ENST00000523596.5:n.490-91A=
NM_001308152.1:c.3284-91A= NP_001295081.1:n.3284-91A=
NM_001308153.1:c.3470-91A= NP_001295082.1:n.3470-91A=
NM_014629.2:c.3398-91A= , LRG_234t1:c.3398-91A= NP_055444.2:n.3398-91A=
NM_014629.3:c.3398-91A= NP_055444.2:n.3398-91A=
XM_005266041.2:c.3401-91A= XP_005266098.1:n.3401-91A=
XM_011534766.1:c.3314-91A= XP_011533068.1:n.3314-91A=
XM_011534767.1:c.3281-91A= XP_011533069.1:n.3281-91A=
XM_011534768.1:c.3401-4135A= XP_011533070.1:n.3401-4135A=
XM_011534769.1:c.3356-91A= XP_011533071.1:n.3356-91A=
XM_005266041.4:c.3401-91A= XP_005266098.1:n.3401-91A=
XM_011534767.2:c.3281-91A= XP_011533069.1:n.3281-91A=
XM_017014003.1:c.3473-91A= XP_016869492.1:n.3473-91A=
XM_024447334.1:c.3401-91A= XP_024303102.1:n.3401-91A=
XM_024447335.1:c.3485-91A= XP_024303103.1:n.3485-91A=
NM_014629.4:c.3398-91A= MANE Select NP_055444.2:n.3398-91A=
NM_001308152.2:c.3284-91A= NP_001295081.1:n.3284-91A=
NM_001308153.2:c.3470-91A= NP_001295082.1:n.3470-91A=