Canonical Allele Identifier: CA9137033

Gene: ARHGEF18

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7466917G>T , CM000681.2:g.7466917G>T	GRCh38
NC_000019.9:g.7531803G>T , CM000681.1:g.7531803G>T	GRCh37
NC_000019.8:g.7437803G>T	NCBI36
NG_047135.1:g.123007G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001367823.1:c.2905-1G>T MANE Select	NP_001354752.1:n.2905-1G>T
ENST00000668164.2:c.2905-1G>T MANE Select	ENSP00000499655.2:n.2905-1G>T
NM_001130955.1:c.2341-1G>T	NP_001124427.1:n.2341-1G>T
NM_001130955.2:c.2179-1G>T	NP_001124427.2:n.2179-1G>T
NM_001367824.1:c.1867-1G>T	NP_001354753.1:n.1867-1G>T
NM_015318.3:c.1867-1G>T	NP_056133.2:n.1867-1G>T
NM_015318.4:c.1867-1G>T	NP_056133.2:n.1867-1G>T
ENST00000319670.13:c.1867-1G>T	ENSP00000319200.7:n.1867-1G>T
ENST00000319670.14:c.1864-1G>T	ENSP00000319200.8:n.1864-1G>T
ENST00000359920.10:c.2341-1G>T	ENSP00000352995.4:n.2341-1G>T
ENST00000359920.11:c.2179-1G>T	ENSP00000352995.5:n.2179-1G>T
ENST00000594665.1:c.1274-1G>T
ENST00000594665.2:c.1867-1G>T	ENSP00000470729.2:n.1867-1G>T
ENST00000617428.2:c.2141-1G>T
ENST00000617428.4:c.1867-1G>T	ENSP00000482647.4:n.1867-1G>T
XM_005272464.3:c.3100-1G>T	XP_005272521.1:n.3100-1G>T
XM_005272464.4:c.3100-1G>T	XP_005272521.1:n.3100-1G>T
XM_006722705.2:c.2905-1G>T	XP_006722768.1:n.2905-1G>T
XM_006722705.3:c.2905-1G>T	XP_006722768.1:n.2905-1G>T
XM_006722706.2:c.2905-1G>T	XP_006722769.1:n.2905-1G>T
XM_006722706.3:c.2905-1G>T	XP_006722769.1:n.2905-1G>T
XM_006722708.2:c.1867-1G>T	XP_006722771.1:n.1867-1G>T
XM_006722709.2:c.1867-1G>T	XP_006722772.1:n.1867-1G>T
XM_011527835.1:c.3100-1G>T	XP_011526137.1:n.3100-1G>T
XM_011527835.2:c.3100-1G>T	XP_011526137.1:n.3100-1G>T
XM_011527836.1:c.3100-1G>T	XP_011526138.1:n.3100-1G>T
XM_011527836.2:c.3100-1G>T	XP_011526138.1:n.3100-1G>T
XM_011527837.1:c.3100-1G>T	XP_011526139.1:n.3100-1G>T
XM_011527837.2:c.3100-1G>T	XP_011526139.1:n.3100-1G>T
XM_011527838.1:c.2905-1G>T	XP_011526140.1:n.2905-1G>T
XM_011527838.3:c.2905-1G>T	XP_011526140.1:n.2905-1G>T
XM_011527839.1:c.2857-1G>T	XP_011526141.1:n.2857-1G>T
XM_011527839.2:c.2857-1G>T	XP_011526141.1:n.2857-1G>T
XM_011527840.1:c.1867-1G>T	XP_011526142.1:n.1867-1G>T
XM_011527840.2:c.1867-1G>T	XP_011526142.1:n.1867-1G>T