Canonical Allele Identifier: CA2320929810
Gene: ARHGEF18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7462240C= , CM000681.2:g.7462240C= GRCh38
NC_000019.9:g.7527126C= , CM000681.1:g.7527126C= GRCh37
NC_000019.8:g.7433126C= NCBI36
NG_047135.1:g.118330C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319670.14:c.1503C= ENSP00000319200.8:p.Leu501=
ENST00000359920.11:c.1815C= ENSP00000352995.5:p.Leu605=
ENST00000594665.2:c.1503C= ENSP00000470729.2:p.Leu501=
ENST00000617428.4:c.1503C= ENSP00000482647.4:p.Leu501=
ENST00000668164.2:c.2541C= MANE Select ENSP00000499655.2:p.Leu847=
ENST00000319670.13:c.1503C= ENSP00000319200.7:p.Leu501=
ENST00000359920.10:c.1977C= ENSP00000352995.4:p.Leu659=
ENST00000594665.1:c.910C=
ENST00000617428.2:c.1777C=
NM_001130955.1:c.1977C= NP_001124427.1:p.Leu659=
NM_015318.3:c.1503C= NP_056133.2:p.Leu501=
XM_005272464.3:c.2736C= XP_005272521.1:p.Leu912=
XM_006722705.2:c.2541C= XP_006722768.1:p.Leu847=
XM_006722706.2:c.2541C= XP_006722769.1:p.Leu847=
XM_006722708.2:c.1503C= XP_006722771.1:p.Leu501=
XM_006722709.2:c.1503C= XP_006722772.1:p.Leu501=
XM_011527835.1:c.2736C= XP_011526137.1:p.Leu912=
XM_011527836.1:c.2736C= XP_011526138.1:p.Leu912=
XM_011527837.1:c.2736C= XP_011526139.1:p.Leu912=
XM_011527838.1:c.2541C= XP_011526140.1:p.Leu847=
XM_011527839.1:c.2493C= XP_011526141.1:p.Leu831=
XM_011527840.1:c.1503C= XP_011526142.1:p.Leu501=
XM_011527841.1:c.2736C= XP_011526143.1:p.Leu912=
XM_005272464.4:c.2736C= XP_005272521.1:p.Leu912=
XM_006722705.3:c.2541C= XP_006722768.1:p.Leu847=
XM_006722706.3:c.2541C= XP_006722769.1:p.Leu847=
XM_011527835.2:c.2736C= XP_011526137.1:p.Leu912=
XM_011527836.2:c.2736C= XP_011526138.1:p.Leu912=
XM_011527837.2:c.2736C= XP_011526139.1:p.Leu912=
XM_011527838.3:c.2541C= XP_011526140.1:p.Leu847=
XM_011527839.2:c.2493C= XP_011526141.1:p.Leu831=
XM_011527840.2:c.1503C= XP_011526142.1:p.Leu501=
XM_011527841.2:c.2736C= XP_011526143.1:p.Leu912=
NM_001130955.2:c.1815C= NP_001124427.2:p.Leu605=
NM_001367823.1:c.2541C= MANE Select NP_001354752.1:p.Leu847=
NM_001367824.1:c.1503C= NP_001354753.1:p.Leu501=
NM_015318.4:c.1503C= NP_056133.2:p.Leu501=