Canonical Allele Identifier: CA413405819
Gene: ARHGEF9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785115C>A , CM000685.2:g.63785115C>A GRCh38
NC_000023.10:g.63004995C>A , CM000685.1:g.63004995C>A GRCh37
NC_000023.9:g.62921720C>A NCBI36
NG_016975.1:g.5432G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000671741.2:c.30+1G>T MANE Select ENSP00000500715.1:n.30+1G>T
ENST00000672467.1:n.99+1G>T
ENST00000374878.5:c.30+1G>T ENSP00000364012.2:n.30+1G>T
ENST00000437457.6:c.30+1G>T ENSP00000399994.3:n.30+1G>T
ENST00000623417.3:c.-118+10401G>T ENSP00000485083.1:n.-118+10401G>T
ENST00000623517.3:c.30+1G>T ENSP00000485369.1:n.30+1G>T
ENST00000624355.1:c.-132+1G>T ENSP00000485327.1:n.-132+1G>T
ENST00000625116.3:c.-195+1G>T ENSP00000485160.1:n.-195+1G>T
NM_001173479.1:c.30+1G>T NP_001166950.1:n.30+1G>T
XM_005262249.1:c.30+1G>T XP_005262306.1:n.30+1G>T
XM_005262252.1:c.-132+1G>T XP_005262309.1:n.-132+1G>T
NM_001330495.1:c.-132+1G>T NP_001317424.1:n.-132+1G>T
NM_001353921.1:c.30+1G>T NP_001340850.1:n.30+1G>T
NM_001353922.1:c.30+1G>T NP_001340851.1:n.30+1G>T
XM_017029378.2:c.30+1G>T XP_016884867.1:n.30+1G>T
XM_024452358.1:c.-132+1G>T XP_024308126.1:n.-132+1G>T
NM_001173479.2:c.30+1G>T NP_001166950.1:n.30+1G>T
NM_001330495.2:c.-132+1G>T NP_001317424.1:n.-132+1G>T
NM_001353921.2:c.30+1G>T MANE Select NP_001340850.1:n.30+1G>T
NM_001353922.2:c.30+1G>T NP_001340851.1:n.30+1G>T
NM_001369043.1:c.-132+1G>T NP_001355972.1:n.-132+1G>T