Canonical Allele Identifier: CA2433164230

Gene: ARHGEF9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785131C= , CM000685.2:g.63785131C=	GRCh38
NC_000023.10:g.63005011C= , CM000685.1:g.63005011C=	GRCh37
NC_000023.9:g.62921736C=	NCBI36
NG_016975.1:g.5416G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000671741.2:c.15G= MANE Select	ENSP00000500715.1:p.Arg5=
ENST00000672467.1:n.84G=
ENST00000374878.5:c.15G=	ENSP00000364012.2:p.Arg5=
ENST00000437457.6:c.15G=	ENSP00000399994.3:p.Arg5=
ENST00000623417.3:c.-118+10385G=	ENSP00000485083.1:n.-118+10385G=
ENST00000623517.3:c.15G=	ENSP00000485369.1:p.Arg5=
ENST00000624355.1:c.-147G=	ENSP00000485327.1:n.-147G=
ENST00000625116.3:c.-210G=	ENSP00000485160.1:n.-210G=
NM_001173479.1:c.15G=	NP_001166950.1:p.Arg5=
XM_005262249.1:c.15G=	XP_005262306.1:p.Arg5=
XM_005262252.1:c.-147G=	XP_005262309.1:n.-147G=
NM_001330495.1:c.-147G=	NP_001317424.1:n.-147G=
NM_001353921.1:c.15G=	NP_001340850.1:p.Arg5=
NM_001353922.1:c.15G=	NP_001340851.1:p.Arg5=
XM_017029378.2:c.15G=	XP_016884867.1:p.Arg5=
XM_024452358.1:c.-147G=	XP_024308126.1:n.-147G=
NM_001173479.2:c.15G=	NP_001166950.1:p.Arg5=
NM_001330495.2:c.-147G=	NP_001317424.1:n.-147G=
NM_001353921.2:c.15G= MANE Select	NP_001340850.1:p.Arg5=
NM_001353922.2:c.15G=	NP_001340851.1:p.Arg5=
NM_001369043.1:c.-147G=	NP_001355972.1:n.-147G=