Canonical Allele Identifier: CA2587934255

Gene: ARHGEF18

Linked Data

• gnomAD v4: 19-7462449-GCTTCTAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7462450_7462456del , CM000681.2:g.7462450_7462456del	GRCh38
NC_000019.9:g.7527336_7527342del , CM000681.1:g.7527336_7527342del	GRCh37
NC_000019.8:g.7433336_7433342del	NCBI36
NG_047135.1:g.118540_118546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319670.14:c.1597+116_1597+122del	ENSP00000319200.8:n.1597+116_1597+122del
ENST00000359920.11:c.1909+116_1909+122del	ENSP00000352995.5:n.1909+116_1909+122del
ENST00000594665.2:c.1597+116_1597+122del	ENSP00000470729.2:n.1597+116_1597+122del
ENST00000617428.4:c.1597+116_1597+122del	ENSP00000482647.4:n.1597+116_1597+122del
ENST00000668164.2:c.2635+116_2635+122del MANE Select	ENSP00000499655.2:n.2635+116_2635+122del
ENST00000319670.13:c.1597+116_1597+122del	ENSP00000319200.7:n.1597+116_1597+122del
ENST00000359920.10:c.2071+116_2071+122del	ENSP00000352995.4:n.2071+116_2071+122del
ENST00000594665.1:c.1004+116_1004+122del
ENST00000617428.2:c.1871+116_1871+122del
NM_001130955.1:c.2071+116_2071+122del	NP_001124427.1:n.2071+116_2071+122del
NM_015318.3:c.1597+116_1597+122del	NP_056133.2:n.1597+116_1597+122del
XM_005272464.3:c.2830+116_2830+122del	XP_005272521.1:n.2830+116_2830+122del
XM_006722705.2:c.2635+116_2635+122del	XP_006722768.1:n.2635+116_2635+122del
XM_006722706.2:c.2635+116_2635+122del	XP_006722769.1:n.2635+116_2635+122del
XM_006722708.2:c.1597+116_1597+122del	XP_006722771.1:n.1597+116_1597+122del
XM_006722709.2:c.1597+116_1597+122del	XP_006722772.1:n.1597+116_1597+122del
XM_011527835.1:c.2830+116_2830+122del	XP_011526137.1:n.2830+116_2830+122del
XM_011527836.1:c.2830+116_2830+122del	XP_011526138.1:n.2830+116_2830+122del
XM_011527837.1:c.2830+116_2830+122del	XP_011526139.1:n.2830+116_2830+122del
XM_011527838.1:c.2635+116_2635+122del	XP_011526140.1:n.2635+116_2635+122del
XM_011527839.1:c.2587+116_2587+122del	XP_011526141.1:n.2587+116_2587+122del
XM_011527840.1:c.1597+116_1597+122del	XP_011526142.1:n.1597+116_1597+122del
XM_011527841.1:c.2830+116_2830+122del	XP_011526143.1:n.2830+116_2830+122del
XM_005272464.4:c.2830+116_2830+122del	XP_005272521.1:n.2830+116_2830+122del
XM_006722705.3:c.2635+116_2635+122del	XP_006722768.1:n.2635+116_2635+122del
XM_006722706.3:c.2635+116_2635+122del	XP_006722769.1:n.2635+116_2635+122del
XM_011527835.2:c.2830+116_2830+122del	XP_011526137.1:n.2830+116_2830+122del
XM_011527836.2:c.2830+116_2830+122del	XP_011526138.1:n.2830+116_2830+122del
XM_011527837.2:c.2830+116_2830+122del	XP_011526139.1:n.2830+116_2830+122del
XM_011527838.3:c.2635+116_2635+122del	XP_011526140.1:n.2635+116_2635+122del
XM_011527839.2:c.2587+116_2587+122del	XP_011526141.1:n.2587+116_2587+122del
XM_011527840.2:c.1597+116_1597+122del	XP_011526142.1:n.1597+116_1597+122del
XM_011527841.2:c.2830+116_2830+122del	XP_011526143.1:n.2830+116_2830+122del
NM_001130955.2:c.1909+116_1909+122del	NP_001124427.2:n.1909+116_1909+122del
NM_001367823.1:c.2635+116_2635+122del MANE Select	NP_001354752.1:n.2635+116_2635+122del
NM_001367824.1:c.1597+116_1597+122del	NP_001354753.1:n.1597+116_1597+122del
NM_015318.4:c.1597+116_1597+122del	NP_056133.2:n.1597+116_1597+122del