Canonical Allele Identifier: CA2433164232

Gene: ARHGEF9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785142G= , CM000685.2:g.63785142G=	GRCh38
NC_000023.10:g.63005022G= , CM000685.1:g.63005022G=	GRCh37
NC_000023.9:g.62921747G=	NCBI36
NG_016975.1:g.5405C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000671741.2:c.4C= MANE Select	ENSP00000500715.1:p.Gln2=
ENST00000672467.1:n.73C=
ENST00000374878.5:c.4C=	ENSP00000364012.2:p.Gln2=
ENST00000437457.6:c.4C=	ENSP00000399994.3:p.Gln2=
ENST00000623417.3:c.-118+10374C=	ENSP00000485083.1:n.-118+10374C=
ENST00000623517.3:c.4C=	ENSP00000485369.1:p.Gln2=
ENST00000624355.1:c.-158C=	ENSP00000485327.1:n.-158C=
ENST00000625116.3:c.-221C=	ENSP00000485160.1:n.-221C=
NM_001173479.1:c.4C=	NP_001166950.1:p.Gln2=
XM_005262249.1:c.4C=	XP_005262306.1:p.Gln2=
XM_005262252.1:c.-158C=	XP_005262309.1:n.-158C=
NM_001330495.1:c.-158C=	NP_001317424.1:n.-158C=
NM_001353921.1:c.4C=	NP_001340850.1:p.Gln2=
NM_001353922.1:c.4C=	NP_001340851.1:p.Gln2=
XM_017029378.2:c.4C=	XP_016884867.1:p.Gln2=
XM_024452358.1:c.-158C=	XP_024308126.1:n.-158C=
NM_001173479.2:c.4C=	NP_001166950.1:p.Gln2=
NM_001330495.2:c.-158C=	NP_001317424.1:n.-158C=
NM_001353921.2:c.4C= MANE Select	NP_001340850.1:p.Gln2=
NM_001353922.2:c.4C=	NP_001340851.1:p.Gln2=
NM_001369043.1:c.-158C=	NP_001355972.1:n.-158C=