Canonical Allele Identifier: CA2320929911

Gene: ARHGEF18

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7462457_7462458delinsGT , CM000681.2:g.7462457_7462458delinsGT	GRCh38
NC_000019.9:g.7527343_7527344delinsGT , CM000681.1:g.7527343_7527344delinsGT	GRCh37
NC_000019.8:g.7433343_7433344delinsGT	NCBI36
NG_047135.1:g.118547_118548delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319670.14:c.1597+123_1597+124delinsGT	ENSP00000319200.8:n.1597+123_1597+124delinsGT
ENST00000359920.11:c.1909+123_1909+124delinsGT	ENSP00000352995.5:n.1909+123_1909+124delinsGT
ENST00000594665.2:c.1597+123_1597+124delinsGT	ENSP00000470729.2:n.1597+123_1597+124delinsGT
ENST00000617428.4:c.1597+123_1597+124delinsGT	ENSP00000482647.4:n.1597+123_1597+124delinsGT
ENST00000668164.2:c.2635+123_2635+124delinsGT MANE Select	ENSP00000499655.2:n.2635+123_2635+124delinsGT
ENST00000319670.13:c.1597+123_1597+124delinsGT	ENSP00000319200.7:n.1597+123_1597+124delinsGT
ENST00000359920.10:c.2071+123_2071+124delinsGT	ENSP00000352995.4:n.2071+123_2071+124delinsGT
ENST00000594665.1:c.1004+123_1004+124delinsGT
ENST00000617428.2:c.1871+123_1871+124delinsGT
NM_001130955.1:c.2071+123_2071+124delinsGT	NP_001124427.1:n.2071+123_2071+124delinsGT
NM_015318.3:c.1597+123_1597+124delinsGT	NP_056133.2:n.1597+123_1597+124delinsGT
XM_005272464.3:c.2830+123_2830+124delinsGT	XP_005272521.1:n.2830+123_2830+124delinsGT
XM_006722705.2:c.2635+123_2635+124delinsGT	XP_006722768.1:n.2635+123_2635+124delinsGT
XM_006722706.2:c.2635+123_2635+124delinsGT	XP_006722769.1:n.2635+123_2635+124delinsGT
XM_006722708.2:c.1597+123_1597+124delinsGT	XP_006722771.1:n.1597+123_1597+124delinsGT
XM_006722709.2:c.1597+123_1597+124delinsGT	XP_006722772.1:n.1597+123_1597+124delinsGT
XM_011527835.1:c.2830+123_2830+124delinsGT	XP_011526137.1:n.2830+123_2830+124delinsGT
XM_011527836.1:c.2830+123_2830+124delinsGT	XP_011526138.1:n.2830+123_2830+124delinsGT
XM_011527837.1:c.2830+123_2830+124delinsGT	XP_011526139.1:n.2830+123_2830+124delinsGT
XM_011527838.1:c.2635+123_2635+124delinsGT	XP_011526140.1:n.2635+123_2635+124delinsGT
XM_011527839.1:c.2587+123_2587+124delinsGT	XP_011526141.1:n.2587+123_2587+124delinsGT
XM_011527840.1:c.1597+123_1597+124delinsGT	XP_011526142.1:n.1597+123_1597+124delinsGT
XM_011527841.1:c.2830+123_2830+124delinsGT	XP_011526143.1:n.2830+123_2830+124delinsGT
XM_005272464.4:c.2830+123_2830+124delinsGT	XP_005272521.1:n.2830+123_2830+124delinsGT
XM_006722705.3:c.2635+123_2635+124delinsGT	XP_006722768.1:n.2635+123_2635+124delinsGT
XM_006722706.3:c.2635+123_2635+124delinsGT	XP_006722769.1:n.2635+123_2635+124delinsGT
XM_011527835.2:c.2830+123_2830+124delinsGT	XP_011526137.1:n.2830+123_2830+124delinsGT
XM_011527836.2:c.2830+123_2830+124delinsGT	XP_011526138.1:n.2830+123_2830+124delinsGT
XM_011527837.2:c.2830+123_2830+124delinsGT	XP_011526139.1:n.2830+123_2830+124delinsGT
XM_011527838.3:c.2635+123_2635+124delinsGT	XP_011526140.1:n.2635+123_2635+124delinsGT
XM_011527839.2:c.2587+123_2587+124delinsGT	XP_011526141.1:n.2587+123_2587+124delinsGT
XM_011527840.2:c.1597+123_1597+124delinsGT	XP_011526142.1:n.1597+123_1597+124delinsGT
XM_011527841.2:c.2830+123_2830+124delinsGT	XP_011526143.1:n.2830+123_2830+124delinsGT
NM_001130955.2:c.1909+123_1909+124delinsGT	NP_001124427.2:n.1909+123_1909+124delinsGT
NM_001367823.1:c.2635+123_2635+124delinsGT MANE Select	NP_001354752.1:n.2635+123_2635+124delinsGT
NM_001367824.1:c.1597+123_1597+124delinsGT	NP_001354753.1:n.1597+123_1597+124delinsGT
NM_015318.4:c.1597+123_1597+124delinsGT	NP_056133.2:n.1597+123_1597+124delinsGT