Canonical Allele Identifier: CA413405833
Gene: ARHGEF9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785120C>G , CM000685.2:g.63785120C>G GRCh38
NC_000023.10:g.63005000C>G , CM000685.1:g.63005000C>G GRCh37
NC_000023.9:g.62921725C>G NCBI36
NG_016975.1:g.5427G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000671741.2:c.26G>C MANE Select ENSP00000500715.1:p.Gly9Ala
ENST00000672467.1:n.95G>C
ENST00000374878.5:c.26G>C ENSP00000364012.2:p.Gly9Ala
ENST00000437457.6:c.26G>C ENSP00000399994.3:p.Gly9Ala
ENST00000623417.3:c.-118+10396G>C ENSP00000485083.1:n.-118+10396G>C
ENST00000623517.3:c.26G>C ENSP00000485369.1:p.Gly9Ala
ENST00000624355.1:c.-136G>C ENSP00000485327.1:n.-136G>C
ENST00000625116.3:c.-199G>C ENSP00000485160.1:n.-199G>C
NM_001173479.1:c.26G>C NP_001166950.1:p.Gly9Ala
XM_005262249.1:c.26G>C XP_005262306.1:p.Gly9Ala
XM_005262252.1:c.-136G>C XP_005262309.1:n.-136G>C
NM_001330495.1:c.-136G>C NP_001317424.1:n.-136G>C
NM_001353921.1:c.26G>C NP_001340850.1:p.Gly9Ala
NM_001353922.1:c.26G>C NP_001340851.1:p.Gly9Ala
XM_017029378.2:c.26G>C XP_016884867.1:p.Gly9Ala
XM_024452358.1:c.-136G>C XP_024308126.1:n.-136G>C
NM_001173479.2:c.26G>C NP_001166950.1:p.Gly9Ala
NM_001330495.2:c.-136G>C NP_001317424.1:n.-136G>C
NM_001353921.2:c.26G>C MANE Select NP_001340850.1:p.Gly9Ala
NM_001353922.2:c.26G>C NP_001340851.1:p.Gly9Ala
NM_001369043.1:c.-136G>C NP_001355972.1:n.-136G>C