Canonical Allele Identifier: CA2433164250
Gene: ARHGEF9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785171G= , CM000685.2:g.63785171G= GRCh38
NC_000023.10:g.63005051G= , CM000685.1:g.63005051G= GRCh37
NC_000023.9:g.62921776G= NCBI36
NG_016975.1:g.5376C=

Transcript Alleles

HGVS Amino-acid change
ENST00000671741.2:c.-26C= MANE Select ENSP00000500715.1:n.-26C=
ENST00000672467.1:n.44C=
ENST00000374878.5:c.-26C= ENSP00000364012.2:n.-26C=
ENST00000437457.6:c.-26C= ENSP00000399994.3:n.-26C=
ENST00000623417.3:c.-118+10345C= ENSP00000485083.1:n.-118+10345C=
ENST00000623517.3:c.-26C= ENSP00000485369.1:n.-26C=
ENST00000624355.1:c.-187C= ENSP00000485327.1:n.-187C=
ENST00000625116.3:c.-250C= ENSP00000485160.1:n.-250C=
NM_001173479.1:c.-26C= NP_001166950.1:n.-26C=
XM_005262249.1:c.-26C= XP_005262306.1:n.-26C=
XM_005262252.1:c.-187C= XP_005262309.1:n.-187C=
NM_001330495.1:c.-187C= NP_001317424.1:n.-187C=
NM_001353921.1:c.-26C= NP_001340850.1:n.-26C=
NM_001353922.1:c.-26C= NP_001340851.1:n.-26C=
XM_017029378.2:c.-26C= XP_016884867.1:n.-26C=
XM_024452358.1:c.-187C= XP_024308126.1:n.-187C=
NM_001173479.2:c.-26C= NP_001166950.1:n.-26C=
NM_001330495.2:c.-187C= NP_001317424.1:n.-187C=
NM_001353921.2:c.-26C= MANE Select NP_001340850.1:n.-26C=
NM_001353922.2:c.-26C= NP_001340851.1:n.-26C=
NM_001369043.1:c.-187C= NP_001355972.1:n.-187C=