Canonical Allele Identifier: CA4601358
Gene: ARHGEF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 518392
dbSNP Id: rs7832438

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1952689A>G , CM000670.2:g.1952689A>G GRCh38
NC_000008.10:g.1900855A>G , CM000670.1:g.1900855A>G GRCh37
NC_000008.9:g.1888262A>G NCBI36
NG_008480.1:g.133707A>G , LRG_234:g.133707A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000349830.8:c.3398-16A>G MANE Select ENSP00000340297.3:p.=
ENST00000635773.1:n.3926-16A>G
ENST00000635855.1:c.*3352-16A>G ENSP00000489726.1:p.=
ENST00000349830.7:c.3398-16A>G ENSP00000340297.3:p.=
ENST00000398564.5:n.3473-16A>G ENSP00000381571.1:p.=
ENST00000518288.5:c.3470-16A>G ENSP00000431012.1:p.=
ENST00000520359.5:c.3284-16A>G ENSP00000427909.1:p.=
ENST00000521927.1:n.235-16A>G
ENST00000522435.5:n.2330-16A>G ENSP00000427768.1:p.=
ENST00000523596.5:n.490-16A>G
NM_001308152.1:c.3284-16A>G NP_001295081.1:p.=
NM_001308153.1:c.3470-16A>G NP_001295082.1:p.=
NM_014629.2:c.3398-16A>G , LRG_234t1:c.3398-16A>G NP_055444.2:p.=
NM_014629.3:c.3398-16A>G NP_055444.2:p.=
XM_005266041.2:c.3401-16A>G XP_005266098.1:p.=
XM_011534766.1:c.3314-16A>G XP_011533068.1:p.=
XM_011534767.1:c.3281-16A>G XP_011533069.1:p.=
XM_011534768.1:c.3401-4060A>G XP_011533070.1:p.=
XM_011534769.1:c.3356-16A>G XP_011533071.1:p.=
XM_005266041.4:c.3401-16A>G XP_005266098.1:p.=
XM_011534767.2:c.3281-16A>G XP_011533069.1:p.=
XM_017014003.1:c.3473-16A>G XP_016869492.1:p.=
XM_024447334.1:c.3401-16A>G XP_024303102.1:p.=
XM_024447335.1:c.3485-16A>G XP_024303103.1:p.=
NM_014629.4:c.3398-16A>G MANE Select NP_055444.2:p.=
NM_001308152.2:c.3284-16A>G NP_001295081.1:p.=
NM_001308153.2:c.3470-16A>G NP_001295082.1:p.=