Canonical Allele Identifier: CA2433164274
Gene: ARHGEF9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785199C= , CM000685.2:g.63785199C= GRCh38
NC_000023.10:g.63005079C= , CM000685.1:g.63005079C= GRCh37
NC_000023.9:g.62921804C= NCBI36
NG_016975.1:g.5348G=

Transcript Alleles

HGVS Amino-acid change
ENST00000671741.2:c.-54G= MANE Select ENSP00000500715.1:n.-54G=
ENST00000672467.1:n.16G=
ENST00000374878.5:c.-54G= ENSP00000364012.2:n.-54G=
ENST00000437457.6:c.-54G= ENSP00000399994.3:n.-54G=
ENST00000623417.3:c.-118+10317G= ENSP00000485083.1:n.-118+10317G=
ENST00000623517.3:c.-54G= ENSP00000485369.1:n.-54G=
ENST00000624355.1:c.-215G= ENSP00000485327.1:n.-215G=
ENST00000625116.3:c.-278G= ENSP00000485160.1:n.-278G=
NM_001173479.1:c.-54G= NP_001166950.1:n.-54G=
XM_005262249.1:c.-54G= XP_005262306.1:n.-54G=
XM_005262252.1:c.-215G= XP_005262309.1:n.-215G=
NM_001330495.1:c.-215G= NP_001317424.1:n.-215G=
NM_001353921.1:c.-54G= NP_001340850.1:n.-54G=
NM_001353922.1:c.-54G= NP_001340851.1:n.-54G=
XM_017029378.2:c.-54G= XP_016884867.1:n.-54G=
XM_024452358.1:c.-215G= XP_024308126.1:n.-215G=
NM_001173479.2:c.-54G= NP_001166950.1:n.-54G=
NM_001330495.2:c.-215G= NP_001317424.1:n.-215G=
NM_001353921.2:c.-54G= MANE Select NP_001340850.1:n.-54G=
NM_001353922.2:c.-54G= NP_001340851.1:n.-54G=
NM_001369043.1:c.-215G= NP_001355972.1:n.-215G=