Canonical Allele Identifier: CA10432029

Gene: ARHGEF9

Linked Data

• dbSNP Id: rs782016092
• ExAC: X:63005059 G / T
• gnomAD v2: X-63005059-G-T
• gnomAD v4: X-63785179-G-T
• MyVariant Identifiers: chrX:g.63005059G>T (hg19) ; chrX:g.63785179G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785179G>T , CM000685.2:g.63785179G>T	GRCh38
NC_000023.10:g.63005059G>T , CM000685.1:g.63005059G>T	GRCh37
NC_000023.9:g.62921784G>T	NCBI36
NG_016975.1:g.5368C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000671741.2:c.-34C>A MANE Select	ENSP00000500715.1:n.-34C>A
ENST00000672467.1:n.36C>A
ENST00000374878.5:c.-34C>A	ENSP00000364012.2:n.-34C>A
ENST00000437457.6:c.-34C>A	ENSP00000399994.3:n.-34C>A
ENST00000623417.3:c.-118+10337C>A	ENSP00000485083.1:n.-118+10337C>A
ENST00000623517.3:c.-34C>A	ENSP00000485369.1:n.-34C>A
ENST00000624355.1:c.-195C>A	ENSP00000485327.1:n.-195C>A
ENST00000625116.3:c.-258C>A	ENSP00000485160.1:n.-258C>A
NM_001173479.1:c.-34C>A	NP_001166950.1:n.-34C>A
XM_005262249.1:c.-34C>A	XP_005262306.1:n.-34C>A
XM_005262252.1:c.-195C>A	XP_005262309.1:n.-195C>A
NM_001330495.1:c.-195C>A	NP_001317424.1:n.-195C>A
NM_001353921.1:c.-34C>A	NP_001340850.1:n.-34C>A
NM_001353922.1:c.-34C>A	NP_001340851.1:n.-34C>A
XM_017029378.2:c.-34C>A	XP_016884867.1:n.-34C>A
XM_024452358.1:c.-195C>A	XP_024308126.1:n.-195C>A
NM_001173479.2:c.-34C>A	NP_001166950.1:n.-34C>A
NM_001330495.2:c.-195C>A	NP_001317424.1:n.-195C>A
NM_001353921.2:c.-34C>A MANE Select	NP_001340850.1:n.-34C>A
NM_001353922.2:c.-34C>A	NP_001340851.1:n.-34C>A
NM_001369043.1:c.-195C>A	NP_001355972.1:n.-195C>A