Canonical Allele Identifier: CA2693909286

Gene: ARHGEF9

Linked Data

• gnomAD v4: X-63785312-T-TCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785313_63785315dup , CM000685.2:g.63785313_63785315dup	GRCh38
NC_000023.10:g.63005193_63005195dup , CM000685.1:g.63005193_63005195dup	GRCh37
NC_000023.9:g.62921918_62921920dup	NCBI36
NG_016975.1:g.5232_5234dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-170_-168dup	ENSP00000364012.2:n.-170_-168dup
ENST00000437457.6:c.-170_-168dup	ENSP00000399994.3:n.-170_-168dup
ENST00000623417.3:c.-118+10201_-118+10203dup	ENSP00000485083.1:n.-118+10201_-118+10203dup
ENST00000623517.3:c.-170_-168dup	ENSP00000485369.1:n.-170_-168dup
NM_001173479.1:c.-170_-168dup	NP_001166950.1:n.-170_-168dup
XM_005262249.1:c.-170_-168dup	XP_005262306.1:n.-170_-168dup
NM_001330495.1:c.-331_-329dup	NP_001317424.1:n.-331_-329dup
NM_001353921.1:c.-170_-168dup	NP_001340850.1:n.-170_-168dup
NM_001353922.1:c.-170_-168dup	NP_001340851.1:n.-170_-168dup
XM_017029378.2:c.-170_-168dup	XP_016884867.1:n.-170_-168dup