Canonical Allele Identifier: CA2693909263

Gene: ARHGEF9

Linked Data

• gnomAD v4: X-63785293-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785293C>T , CM000685.2:g.63785293C>T	GRCh38
NC_000023.10:g.63005173C>T , CM000685.1:g.63005173C>T	GRCh37
NC_000023.9:g.62921898C>T	NCBI36
NG_016975.1:g.5254G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-148G>A	ENSP00000364012.2:n.-148G>A
ENST00000437457.6:c.-148G>A	ENSP00000399994.3:n.-148G>A
ENST00000623417.3:c.-118+10223G>A	ENSP00000485083.1:n.-118+10223G>A
ENST00000623517.3:c.-148G>A	ENSP00000485369.1:n.-148G>A
NM_001173479.1:c.-148G>A	NP_001166950.1:n.-148G>A
XM_005262249.1:c.-148G>A	XP_005262306.1:n.-148G>A
NM_001330495.1:c.-309G>A	NP_001317424.1:n.-309G>A
NM_001353921.1:c.-148G>A	NP_001340850.1:n.-148G>A
NM_001353922.1:c.-148G>A	NP_001340851.1:n.-148G>A
XM_017029378.2:c.-148G>A	XP_016884867.1:n.-148G>A