Canonical Allele Identifier: CA516873536

Gene: ARHGEF9

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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