Canonical Allele Identifier: CA358247
Gene: ARHGEF9 HGNC NCBI

Linked Data

ClinVar Variation Id: 225050
ClinVar RCV Id: RCV000210722
dbSNP Id: rs869312941

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63665930G>A , CM000685.2:g.63665930G>A GRCh38
NC_000023.10:g.62885810G>A , CM000685.1:g.62885810G>A GRCh37
NC_000023.9:g.62802535G>A NCBI36
NG_016975.1:g.124617C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000624538.2:c.949C>T ENSP00000485282.2:p.Arg317Trp
ENST00000635729.1:c.1051C>T ENSP00000490940.1:p.Arg351Trp
ENST00000635967.1:c.949C>T ENSP00000490691.1:p.Arg317Trp
ENST00000636048.1:c.949C>T ENSP00000490063.1:p.Arg317Trp
ENST00000636102.1:c.*890C>T ENSP00000490693.1:p.=
ENST00000636276.1:c.949C>T ENSP00000490408.1:p.Arg317Trp
ENST00000636392.1:c.949C>T ENSP00000489853.1:p.Arg317Trp
ENST00000636926.1:c.1012C>T ENSP00000490667.1:p.Arg338Trp
ENST00000637040.1:c.826C>T ENSP00000490459.1:p.Arg276Trp
ENST00000637178.1:c.949C>T ENSP00000489862.1:p.Arg317Trp
ENST00000637417.1:c.949C>T ENSP00000490269.1:p.Arg317Trp
ENST00000637520.1:c.949C>T ENSP00000490123.1:p.Arg317Trp
ENST00000637557.1:c.949C>T ENSP00000490679.1:p.Arg317Trp
ENST00000637723.2:c.949C>T ENSP00000489637.2:p.Arg317Trp
ENST00000637855.1:n.734C>T
ENST00000638021.1:c.949C>T ENSP00000490410.1:p.Arg317Trp
ENST00000639092.1:c.*910C>T ENSP00000492318.1:p.=
ENST00000671741.2:c.1033C>T MANE Select ENSP00000500715.1:p.Arg345Trp
ENST00000671907.1:c.1012C>T ENSP00000500829.1:p.Arg338Trp
ENST00000672194.1:c.931C>T ENSP00000499905.1:p.Arg311Trp
ENST00000672467.1:n.1102C>T
ENST00000672513.1:c.861+8108C>T ENSP00000500825.1:p.=
ENST00000253401.10:c.1012C>T ENSP00000253401.6:p.Arg338Trp
ENST00000374870.8:c.1012C>T ENSP00000364004.5:p.Arg338Trp
ENST00000374872.4:c.949C>T ENSP00000364006.1:p.Arg317Trp
ENST00000374878.5:c.1033C>T ENSP00000364012.2:p.Arg345Trp
ENST00000437457.6:c.1033C>T ENSP00000399994.3:p.Arg345Trp
ENST00000466925.4:n.189C>T
ENST00000495564.5:c.*781+8108C>T ENSP00000485633.1:p.=
ENST00000623517.3:c.853C>T ENSP00000485369.1:p.Arg285Trp
ENST00000624210.3:c.949C>T ENSP00000485144.1:p.Arg317Trp
ENST00000624843.3:c.706C>T ENSP00000485626.1:p.Arg236Trp
NM_001173479.1:c.853C>T NP_001166950.1:p.Arg285Trp
NM_001173480.1:c.706C>T NP_001166951.1:p.Arg236Trp
NM_015185.2:c.1012C>T NP_056000.1:p.Arg338Trp
XM_005262249.1:c.1033C>T XP_005262306.1:p.Arg345Trp
XM_005262250.3:c.949C>T XP_005262307.1:p.Arg317Trp
XM_005262251.1:c.949C>T XP_005262308.1:p.Arg317Trp
XM_005262252.1:c.949C>T XP_005262309.1:p.Arg317Trp
XM_011530890.1:c.1012C>T XP_011529192.1:p.Arg338Trp
XM_011530891.1:c.861+8108C>T XP_011529193.1:p.=
XM_011530892.1:c.832C>T XP_011529194.1:p.Arg278Trp
NM_001330495.1:c.949C>T NP_001317424.1:p.Arg317Trp
NM_001353921.1:c.1033C>T NP_001340850.1:p.Arg345Trp
NM_001353922.1:c.945+8108C>T NP_001340851.1:p.=
NM_001353923.1:c.1051C>T NP_001340852.1:p.Arg351Trp
NM_001353924.1:c.832C>T NP_001340853.1:p.Arg278Trp
NM_001353926.1:c.832C>T NP_001340855.1:p.Arg278Trp
NM_001353927.1:c.861+8108C>T NP_001340856.1:p.=
NM_001353928.1:c.924+8108C>T NP_001340857.1:p.=
XM_005262250.4:c.949C>T XP_005262307.1:p.Arg317Trp
XM_017029364.1:c.1027C>T XP_016884853.1:p.Arg343Trp
XM_017029366.1:c.1012C>T XP_016884855.1:p.Arg338Trp
XM_017029367.1:c.949C>T XP_016884856.1:p.Arg317Trp
XM_017029368.2:c.949C>T XP_016884857.1:p.Arg317Trp
XM_017029372.1:c.861+8108C>T XP_016884861.1:p.=
XM_017029373.2:c.706C>T XP_016884862.1:p.Arg236Trp
XM_017029374.2:c.744+8108C>T XP_016884863.1:p.=
XM_017029377.2:c.1012C>T XP_016884866.1:p.Arg338Trp
XM_017029378.2:c.1033C>T XP_016884867.1:p.Arg345Trp
XM_017029379.1:c.949C>T XP_016884868.1:p.Arg317Trp
XM_017029380.2:c.832C>T XP_016884869.1:p.Arg278Trp
XM_024452356.1:c.1006C>T XP_024308124.1:p.Arg336Trp
XM_024452357.1:c.949C>T XP_024308125.1:p.Arg317Trp
XM_024452358.1:c.949C>T XP_024308126.1:p.Arg317Trp
NM_001173479.2:c.853C>T NP_001166950.1:p.Arg285Trp
NM_001173480.2:c.706C>T NP_001166951.1:p.Arg236Trp
NM_001330495.2:c.949C>T NP_001317424.1:p.Arg317Trp
NM_001353921.2:c.1033C>T MANE Select NP_001340850.1:p.Arg345Trp
NM_001353922.2:c.945+8108C>T NP_001340851.1:p.=
NM_001353924.2:c.832C>T NP_001340853.1:p.Arg278Trp
NM_001353926.2:c.832C>T NP_001340855.1:p.Arg278Trp
NM_001353927.2:c.861+8108C>T NP_001340856.1:p.=
NM_001353928.2:c.924+8108C>T NP_001340857.1:p.=
NM_001369030.1:c.1012C>T NP_001355959.1:p.Arg338Trp
NM_001369031.1:c.1012C>T NP_001355960.1:p.Arg338Trp
NM_001369032.1:c.1012C>T NP_001355961.1:p.Arg338Trp
NM_001369033.1:c.949C>T NP_001355962.1:p.Arg317Trp
NM_001369034.1:c.949C>T NP_001355963.1:p.Arg317Trp
NM_001369035.1:c.949C>T NP_001355964.1:p.Arg317Trp
NM_001369036.1:c.949C>T NP_001355965.1:p.Arg317Trp
NM_001369037.1:c.949C>T NP_001355966.1:p.Arg317Trp
NM_001369038.1:c.949C>T NP_001355967.1:p.Arg317Trp
NM_001369039.1:c.832C>T NP_001355968.1:p.Arg278Trp
NM_001369040.1:c.832C>T NP_001355969.1:p.Arg278Trp
NM_001369041.1:c.861+8108C>T NP_001355970.1:p.=
NM_001369042.1:c.706C>T NP_001355971.1:p.Arg236Trp
NM_001369043.1:c.949C>T NP_001355972.1:p.Arg317Trp
NM_001369044.1:c.949C>T NP_001355973.1:p.Arg317Trp
NM_001369045.1:c.510+8108C>T NP_001355974.1:p.=
NM_015185.3:c.1012C>T NP_056000.1:p.Arg338Trp