Canonical Allele Identifier: CA516873535
Gene: ARHGEF9 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.63004999T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785119T>C , CM000685.2:g.63785119T>C GRCh38
NC_000023.10:g.63004999T>C , CM000685.1:g.63004999T>C GRCh37
NC_000023.9:g.62921724T>C NCBI36
NG_016975.1:g.5428A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000671741.2:c.27A>G MANE Select ENSP00000500715.1:p.Gly9=
ENST00000672467.1:n.96A>G
ENST00000374878.5:c.27A>G ENSP00000364012.2:p.Gly9=
ENST00000437457.6:c.27A>G ENSP00000399994.3:p.Gly9=
ENST00000623417.3:c.-118+10397A>G ENSP00000485083.1:n.-118+10397A>G
ENST00000623517.3:c.27A>G ENSP00000485369.1:p.Gly9=
ENST00000624355.1:c.-135A>G ENSP00000485327.1:n.-135A>G
ENST00000625116.3:c.-198A>G ENSP00000485160.1:n.-198A>G
NM_001173479.1:c.27A>G NP_001166950.1:p.Gly9=
XM_005262249.1:c.27A>G XP_005262306.1:p.Gly9=
XM_005262252.1:c.-135A>G XP_005262309.1:n.-135A>G
NM_001330495.1:c.-135A>G NP_001317424.1:n.-135A>G
NM_001353921.1:c.27A>G NP_001340850.1:p.Gly9=
NM_001353922.1:c.27A>G NP_001340851.1:p.Gly9=
XM_017029378.2:c.27A>G XP_016884867.1:p.Gly9=
XM_024452358.1:c.-135A>G XP_024308126.1:n.-135A>G
NM_001173479.2:c.27A>G NP_001166950.1:p.Gly9=
NM_001330495.2:c.-135A>G NP_001317424.1:n.-135A>G
NM_001353921.2:c.27A>G MANE Select NP_001340850.1:p.Gly9=
NM_001353922.2:c.27A>G NP_001340851.1:p.Gly9=
NM_001369043.1:c.-135A>G NP_001355972.1:n.-135A>G