Canonical Allele Identifier: CA2320929878

Gene: ARHGEF18

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7462413_7462414delinsCT , CM000681.2:g.7462413_7462414delinsCT	GRCh38
NC_000019.9:g.7527299_7527300delinsCT , CM000681.1:g.7527299_7527300delinsCT	GRCh37
NC_000019.8:g.7433299_7433300delinsCT	NCBI36
NG_047135.1:g.118503_118504delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319670.14:c.1597+79_1597+80delinsCT	ENSP00000319200.8:n.1597+79_1597+80delinsCT
ENST00000359920.11:c.1909+79_1909+80delinsCT	ENSP00000352995.5:n.1909+79_1909+80delinsCT
ENST00000594665.2:c.1597+79_1597+80delinsCT	ENSP00000470729.2:n.1597+79_1597+80delinsCT
ENST00000617428.4:c.1597+79_1597+80delinsCT	ENSP00000482647.4:n.1597+79_1597+80delinsCT
ENST00000668164.2:c.2635+79_2635+80delinsCT MANE Select	ENSP00000499655.2:n.2635+79_2635+80delinsCT
ENST00000319670.13:c.1597+79_1597+80delinsCT	ENSP00000319200.7:n.1597+79_1597+80delinsCT
ENST00000359920.10:c.2071+79_2071+80delinsCT	ENSP00000352995.4:n.2071+79_2071+80delinsCT
ENST00000594665.1:c.1004+79_1004+80delinsCT
ENST00000617428.2:c.1871+79_1871+80delinsCT
NM_001130955.1:c.2071+79_2071+80delinsCT	NP_001124427.1:n.2071+79_2071+80delinsCT
NM_015318.3:c.1597+79_1597+80delinsCT	NP_056133.2:n.1597+79_1597+80delinsCT
XM_005272464.3:c.2830+79_2830+80delinsCT	XP_005272521.1:n.2830+79_2830+80delinsCT
XM_006722705.2:c.2635+79_2635+80delinsCT	XP_006722768.1:n.2635+79_2635+80delinsCT
XM_006722706.2:c.2635+79_2635+80delinsCT	XP_006722769.1:n.2635+79_2635+80delinsCT
XM_006722708.2:c.1597+79_1597+80delinsCT	XP_006722771.1:n.1597+79_1597+80delinsCT
XM_006722709.2:c.1597+79_1597+80delinsCT	XP_006722772.1:n.1597+79_1597+80delinsCT
XM_011527835.1:c.2830+79_2830+80delinsCT	XP_011526137.1:n.2830+79_2830+80delinsCT
XM_011527836.1:c.2830+79_2830+80delinsCT	XP_011526138.1:n.2830+79_2830+80delinsCT
XM_011527837.1:c.2830+79_2830+80delinsCT	XP_011526139.1:n.2830+79_2830+80delinsCT
XM_011527838.1:c.2635+79_2635+80delinsCT	XP_011526140.1:n.2635+79_2635+80delinsCT
XM_011527839.1:c.2587+79_2587+80delinsCT	XP_011526141.1:n.2587+79_2587+80delinsCT
XM_011527840.1:c.1597+79_1597+80delinsCT	XP_011526142.1:n.1597+79_1597+80delinsCT
XM_011527841.1:c.2830+79_2830+80delinsCT	XP_011526143.1:n.2830+79_2830+80delinsCT
XM_005272464.4:c.2830+79_2830+80delinsCT	XP_005272521.1:n.2830+79_2830+80delinsCT
XM_006722705.3:c.2635+79_2635+80delinsCT	XP_006722768.1:n.2635+79_2635+80delinsCT
XM_006722706.3:c.2635+79_2635+80delinsCT	XP_006722769.1:n.2635+79_2635+80delinsCT
XM_011527835.2:c.2830+79_2830+80delinsCT	XP_011526137.1:n.2830+79_2830+80delinsCT
XM_011527836.2:c.2830+79_2830+80delinsCT	XP_011526138.1:n.2830+79_2830+80delinsCT
XM_011527837.2:c.2830+79_2830+80delinsCT	XP_011526139.1:n.2830+79_2830+80delinsCT
XM_011527838.3:c.2635+79_2635+80delinsCT	XP_011526140.1:n.2635+79_2635+80delinsCT
XM_011527839.2:c.2587+79_2587+80delinsCT	XP_011526141.1:n.2587+79_2587+80delinsCT
XM_011527840.2:c.1597+79_1597+80delinsCT	XP_011526142.1:n.1597+79_1597+80delinsCT
XM_011527841.2:c.2830+79_2830+80delinsCT	XP_011526143.1:n.2830+79_2830+80delinsCT
NM_001130955.2:c.1909+79_1909+80delinsCT	NP_001124427.2:n.1909+79_1909+80delinsCT
NM_001367823.1:c.2635+79_2635+80delinsCT MANE Select	NP_001354752.1:n.2635+79_2635+80delinsCT
NM_001367824.1:c.1597+79_1597+80delinsCT	NP_001354753.1:n.1597+79_1597+80delinsCT
NM_015318.4:c.1597+79_1597+80delinsCT	NP_056133.2:n.1597+79_1597+80delinsCT