Canonical Allele Identifier: CA2433164214

Gene: ARHGEF9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785095G= , CM000685.2:g.63785095G=	GRCh38
NC_000023.10:g.63004975G= , CM000685.1:g.63004975G=	GRCh37
NC_000023.9:g.62921700G=	NCBI36
NG_016975.1:g.5452C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000671741.2:c.30+21C= MANE Select	ENSP00000500715.1:n.30+21C=
ENST00000672467.1:n.99+21C=
ENST00000374878.5:c.30+21C=	ENSP00000364012.2:n.30+21C=
ENST00000437457.6:c.30+21C=	ENSP00000399994.3:n.30+21C=
ENST00000623417.3:c.-118+10421C=	ENSP00000485083.1:n.-118+10421C=
ENST00000623517.3:c.30+21C=	ENSP00000485369.1:n.30+21C=
ENST00000624355.1:c.-132+21C=	ENSP00000485327.1:n.-132+21C=
ENST00000625116.3:c.-195+21C=	ENSP00000485160.1:n.-195+21C=
NM_001173479.1:c.30+21C=	NP_001166950.1:n.30+21C=
XM_005262249.1:c.30+21C=	XP_005262306.1:n.30+21C=
XM_005262252.1:c.-132+21C=	XP_005262309.1:n.-132+21C=
NM_001330495.1:c.-132+21C=	NP_001317424.1:n.-132+21C=
NM_001353921.1:c.30+21C=	NP_001340850.1:n.30+21C=
NM_001353922.1:c.30+21C=	NP_001340851.1:n.30+21C=
XM_017029378.2:c.30+21C=	XP_016884867.1:n.30+21C=
XM_024452358.1:c.-132+21C=	XP_024308126.1:n.-132+21C=
NM_001173479.2:c.30+21C=	NP_001166950.1:n.30+21C=
NM_001330495.2:c.-132+21C=	NP_001317424.1:n.-132+21C=
NM_001353921.2:c.30+21C= MANE Select	NP_001340850.1:n.30+21C=
NM_001353922.2:c.30+21C=	NP_001340851.1:n.30+21C=
NM_001369043.1:c.-132+21C=	NP_001355972.1:n.-132+21C=