Canonical Allele Identifier: CA413405846

Gene: ARHGEF9

Linked Data

• MyVariant Identifiers: chrX:g.63005007C>G (hg19) ; chrX:g.63785127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785127C>G , CM000685.2:g.63785127C>G	GRCh38
NC_000023.10:g.63005007C>G , CM000685.1:g.63005007C>G	GRCh37
NC_000023.9:g.62921732C>G	NCBI36
NG_016975.1:g.5420G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000671741.2:c.19G>C MANE Select	ENSP00000500715.1:p.Gly7Arg
ENST00000672467.1:n.88G>C
ENST00000374878.5:c.19G>C	ENSP00000364012.2:p.Gly7Arg
ENST00000437457.6:c.19G>C	ENSP00000399994.3:p.Gly7Arg
ENST00000623417.3:c.-118+10389G>C	ENSP00000485083.1:n.-118+10389G>C
ENST00000623517.3:c.19G>C	ENSP00000485369.1:p.Gly7Arg
ENST00000624355.1:c.-143G>C	ENSP00000485327.1:n.-143G>C
ENST00000625116.3:c.-206G>C	ENSP00000485160.1:n.-206G>C
NM_001173479.1:c.19G>C	NP_001166950.1:p.Gly7Arg
XM_005262249.1:c.19G>C	XP_005262306.1:p.Gly7Arg
XM_005262252.1:c.-143G>C	XP_005262309.1:n.-143G>C
NM_001330495.1:c.-143G>C	NP_001317424.1:n.-143G>C
NM_001353921.1:c.19G>C	NP_001340850.1:p.Gly7Arg
NM_001353922.1:c.19G>C	NP_001340851.1:p.Gly7Arg
XM_017029378.2:c.19G>C	XP_016884867.1:p.Gly7Arg
XM_024452358.1:c.-143G>C	XP_024308126.1:n.-143G>C
NM_001173479.2:c.19G>C	NP_001166950.1:p.Gly7Arg
NM_001330495.2:c.-143G>C	NP_001317424.1:n.-143G>C
NM_001353921.2:c.19G>C MANE Select	NP_001340850.1:p.Gly7Arg
NM_001353922.2:c.19G>C	NP_001340851.1:p.Gly7Arg
NM_001369043.1:c.-143G>C	NP_001355972.1:n.-143G>C