Canonical Allele Identifier: CA2320929820
Gene: ARHGEF18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7462257C= , CM000681.2:g.7462257C= GRCh38
NC_000019.9:g.7527143C= , CM000681.1:g.7527143C= GRCh37
NC_000019.8:g.7433143C= NCBI36
NG_047135.1:g.118347C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319670.14:c.1520C= ENSP00000319200.8:p.Pro507=
ENST00000359920.11:c.1832C= ENSP00000352995.5:p.Pro611=
ENST00000594665.2:c.1520C= ENSP00000470729.2:p.Pro507=
ENST00000617428.4:c.1520C= ENSP00000482647.4:p.Pro507=
ENST00000668164.2:c.2558C= MANE Select ENSP00000499655.2:p.Pro853=
ENST00000319670.13:c.1520C= ENSP00000319200.7:p.Pro507=
ENST00000359920.10:c.1994C= ENSP00000352995.4:p.Pro665=
ENST00000594665.1:c.927C=
ENST00000617428.2:c.1794C=
NM_001130955.1:c.1994C= NP_001124427.1:p.Pro665=
NM_015318.3:c.1520C= NP_056133.2:p.Pro507=
XM_005272464.3:c.2753C= XP_005272521.1:p.Pro918=
XM_006722705.2:c.2558C= XP_006722768.1:p.Pro853=
XM_006722706.2:c.2558C= XP_006722769.1:p.Pro853=
XM_006722708.2:c.1520C= XP_006722771.1:p.Pro507=
XM_006722709.2:c.1520C= XP_006722772.1:p.Pro507=
XM_011527835.1:c.2753C= XP_011526137.1:p.Pro918=
XM_011527836.1:c.2753C= XP_011526138.1:p.Pro918=
XM_011527837.1:c.2753C= XP_011526139.1:p.Pro918=
XM_011527838.1:c.2558C= XP_011526140.1:p.Pro853=
XM_011527839.1:c.2510C= XP_011526141.1:p.Pro837=
XM_011527840.1:c.1520C= XP_011526142.1:p.Pro507=
XM_011527841.1:c.2753C= XP_011526143.1:p.Pro918=
XM_005272464.4:c.2753C= XP_005272521.1:p.Pro918=
XM_006722705.3:c.2558C= XP_006722768.1:p.Pro853=
XM_006722706.3:c.2558C= XP_006722769.1:p.Pro853=
XM_011527835.2:c.2753C= XP_011526137.1:p.Pro918=
XM_011527836.2:c.2753C= XP_011526138.1:p.Pro918=
XM_011527837.2:c.2753C= XP_011526139.1:p.Pro918=
XM_011527838.3:c.2558C= XP_011526140.1:p.Pro853=
XM_011527839.2:c.2510C= XP_011526141.1:p.Pro837=
XM_011527840.2:c.1520C= XP_011526142.1:p.Pro507=
XM_011527841.2:c.2753C= XP_011526143.1:p.Pro918=
NM_001130955.2:c.1832C= NP_001124427.2:p.Pro611=
NM_001367823.1:c.2558C= MANE Select NP_001354752.1:p.Pro853=
NM_001367824.1:c.1520C= NP_001354753.1:p.Pro507=
NM_015318.4:c.1520C= NP_056133.2:p.Pro507=