Canonical Allele Identifier: CA259716
Gene: ARHGEF9 HGNC NCBI

Linked Data

ClinVar Variation Id: 29968
ClinVar RCV Id: RCV000022860
dbSNP Id: rs397514460

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785142G>A , CM000685.2:g.63785142G>A GRCh38
NC_000023.10:g.63005022G>A , CM000685.1:g.63005022G>A GRCh37
NC_000023.9:g.62921747G>A NCBI36
NG_016975.1:g.5405C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000671741.2:c.4C>T MANE Select ENSP00000500715.1:p.Gln2Ter
ENST00000672467.1:n.73C>T
ENST00000374878.5:c.4C>T ENSP00000364012.2:p.Gln2Ter
ENST00000437457.6:c.4C>T ENSP00000399994.3:p.Gln2Ter
ENST00000623417.3:c.-118+10374C>T ENSP00000485083.1:p.=
ENST00000623517.3:c.4C>T ENSP00000485369.1:p.Gln2Ter
ENST00000624355.1:c.-158C>T ENSP00000485327.1:p.=
ENST00000625116.3:c.-221C>T ENSP00000485160.1:p.=
NM_001173479.1:c.4C>T NP_001166950.1:p.Gln2Ter
XM_005262249.1:c.4C>T XP_005262306.1:p.Gln2Ter
XM_005262252.1:c.-158C>T XP_005262309.1:p.=
NM_001330495.1:c.-158C>T NP_001317424.1:p.=
NM_001353921.1:c.4C>T NP_001340850.1:p.Gln2Ter
NM_001353922.1:c.4C>T NP_001340851.1:p.Gln2Ter
XM_017029378.2:c.4C>T XP_016884867.1:p.Gln2Ter
XM_024452358.1:c.-158C>T XP_024308126.1:p.=
NM_001173479.2:c.4C>T NP_001166950.1:p.Gln2Ter
NM_001330495.2:c.-158C>T NP_001317424.1:p.=
NM_001353921.2:c.4C>T MANE Select NP_001340850.1:p.Gln2Ter
NM_001353922.2:c.4C>T NP_001340851.1:p.Gln2Ter
NM_001369043.1:c.-158C>T NP_001355972.1:p.=