Canonical Allele Identifier: CA2693909321

Gene: ARHGEF9

Linked Data

• gnomAD v4: X-63785348-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785349_63785350del , CM000685.2:g.63785349_63785350del	GRCh38
NC_000023.10:g.63005229_63005230del , CM000685.1:g.63005229_63005230del	GRCh37
NC_000023.9:g.62921954_62921955del	NCBI36
NG_016975.1:g.5197_5198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-205_-204del	ENSP00000364012.2:n.-205_-204del
ENST00000437457.6:c.-205_-204del	ENSP00000399994.3:n.-205_-204del
ENST00000623417.3:c.-118+10166_-118+10167del	ENSP00000485083.1:n.-118+10166_-118+10167del
ENST00000623517.3:c.-205_-204del	ENSP00000485369.1:n.-205_-204del
NM_001173479.1:c.-205_-204del	NP_001166950.1:n.-205_-204del
XM_005262249.1:c.-205_-204del	XP_005262306.1:n.-205_-204del
NM_001330495.1:c.-366_-365del	NP_001317424.1:n.-366_-365del
NM_001353921.1:c.-205_-204del	NP_001340850.1:n.-205_-204del
NM_001353922.1:c.-205_-204del	NP_001340851.1:n.-205_-204del
XM_017029378.2:c.-205_-204del	XP_016884867.1:n.-205_-204del