Canonical Allele Identifier: CA2433164321

Gene: ARHGEF9

Linked Data

• dbSNP Id: rs2056444026

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785279_63785280insGAG , CM000685.2:g.63785279_63785280insGAG	GRCh38
NC_000023.10:g.63005159_63005160insGAG , CM000685.1:g.63005159_63005160insGAG	GRCh37
NC_000023.9:g.62921884_62921885insGAG	NCBI36
NG_016975.1:g.5267_5268insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-135_-134insCTC	ENSP00000364012.2:n.-135_-134insCTC
ENST00000437457.6:c.-135_-134insCTC	ENSP00000399994.3:n.-135_-134insCTC
ENST00000623417.3:c.-118+10236_-118+10237insCTC	ENSP00000485083.1:n.-118+10236_-118+10237insCTC
ENST00000623517.3:c.-135_-134insCTC	ENSP00000485369.1:n.-135_-134insCTC
NM_001173479.1:c.-135_-134insCTC	NP_001166950.1:n.-135_-134insCTC
XM_005262249.1:c.-135_-134insCTC	XP_005262306.1:n.-135_-134insCTC
NM_001330495.1:c.-296_-295insCTC	NP_001317424.1:n.-296_-295insCTC
NM_001353921.1:c.-135_-134insCTC	NP_001340850.1:n.-135_-134insCTC
NM_001353922.1:c.-135_-134insCTC	NP_001340851.1:n.-135_-134insCTC
XM_017029378.2:c.-135_-134insCTC	XP_016884867.1:n.-135_-134insCTC