Canonical Allele Identifier: CA2320929896

Gene: ARHGEF18

Linked Data

• dbSNP Id: rs1976332435

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7462431_7462434del , CM000681.2:g.7462431_7462434del	GRCh38
NC_000019.9:g.7527317_7527320del , CM000681.1:g.7527317_7527320del	GRCh37
NC_000019.8:g.7433317_7433320del	NCBI36
NG_047135.1:g.118521_118524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319670.14:c.1597+97_1597+100del	ENSP00000319200.8:n.1597+97_1597+100del
ENST00000359920.11:c.1909+97_1909+100del	ENSP00000352995.5:n.1909+97_1909+100del
ENST00000594665.2:c.1597+97_1597+100del	ENSP00000470729.2:n.1597+97_1597+100del
ENST00000617428.4:c.1597+97_1597+100del	ENSP00000482647.4:n.1597+97_1597+100del
ENST00000668164.2:c.2635+97_2635+100del MANE Select	ENSP00000499655.2:n.2635+97_2635+100del
ENST00000319670.13:c.1597+97_1597+100del	ENSP00000319200.7:n.1597+97_1597+100del
ENST00000359920.10:c.2071+97_2071+100del	ENSP00000352995.4:n.2071+97_2071+100del
ENST00000594665.1:c.1004+97_1004+100del
ENST00000617428.2:c.1871+97_1871+100del
NM_001130955.1:c.2071+97_2071+100del	NP_001124427.1:n.2071+97_2071+100del
NM_015318.3:c.1597+97_1597+100del	NP_056133.2:n.1597+97_1597+100del
XM_005272464.3:c.2830+97_2830+100del	XP_005272521.1:n.2830+97_2830+100del
XM_006722705.2:c.2635+97_2635+100del	XP_006722768.1:n.2635+97_2635+100del
XM_006722706.2:c.2635+97_2635+100del	XP_006722769.1:n.2635+97_2635+100del
XM_006722708.2:c.1597+97_1597+100del	XP_006722771.1:n.1597+97_1597+100del
XM_006722709.2:c.1597+97_1597+100del	XP_006722772.1:n.1597+97_1597+100del
XM_011527835.1:c.2830+97_2830+100del	XP_011526137.1:n.2830+97_2830+100del
XM_011527836.1:c.2830+97_2830+100del	XP_011526138.1:n.2830+97_2830+100del
XM_011527837.1:c.2830+97_2830+100del	XP_011526139.1:n.2830+97_2830+100del
XM_011527838.1:c.2635+97_2635+100del	XP_011526140.1:n.2635+97_2635+100del
XM_011527839.1:c.2587+97_2587+100del	XP_011526141.1:n.2587+97_2587+100del
XM_011527840.1:c.1597+97_1597+100del	XP_011526142.1:n.1597+97_1597+100del
XM_011527841.1:c.2830+97_2830+100del	XP_011526143.1:n.2830+97_2830+100del
XM_005272464.4:c.2830+97_2830+100del	XP_005272521.1:n.2830+97_2830+100del
XM_006722705.3:c.2635+97_2635+100del	XP_006722768.1:n.2635+97_2635+100del
XM_006722706.3:c.2635+97_2635+100del	XP_006722769.1:n.2635+97_2635+100del
XM_011527835.2:c.2830+97_2830+100del	XP_011526137.1:n.2830+97_2830+100del
XM_011527836.2:c.2830+97_2830+100del	XP_011526138.1:n.2830+97_2830+100del
XM_011527837.2:c.2830+97_2830+100del	XP_011526139.1:n.2830+97_2830+100del
XM_011527838.3:c.2635+97_2635+100del	XP_011526140.1:n.2635+97_2635+100del
XM_011527839.2:c.2587+97_2587+100del	XP_011526141.1:n.2587+97_2587+100del
XM_011527840.2:c.1597+97_1597+100del	XP_011526142.1:n.1597+97_1597+100del
XM_011527841.2:c.2830+97_2830+100del	XP_011526143.1:n.2830+97_2830+100del
NM_001130955.2:c.1909+97_1909+100del	NP_001124427.2:n.1909+97_1909+100del
NM_001367823.1:c.2635+97_2635+100del MANE Select	NP_001354752.1:n.2635+97_2635+100del
NM_001367824.1:c.1597+97_1597+100del	NP_001354753.1:n.1597+97_1597+100del
NM_015318.4:c.1597+97_1597+100del	NP_056133.2:n.1597+97_1597+100del