Canonical Allele Identifier: CA657704485

Gene: ARHGEF9

Linked Data

• COSMIC: COSN19672033

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785198_63785199insA , CM000685.2:g.63785198_63785199insA	GRCh38
NC_000023.10:g.63005078_63005079insA , CM000685.1:g.63005078_63005079insA	GRCh37
NC_000023.9:g.62921803_62921804insA	NCBI36
NG_016975.1:g.5348_5349insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000671741.2:c.-54_-53insT MANE Select	ENSP00000500715.1:n.-54_-53insT
ENST00000672467.1:n.16_17insT
ENST00000374878.5:c.-54_-53insT	ENSP00000364012.2:n.-54_-53insT
ENST00000437457.6:c.-54_-53insT	ENSP00000399994.3:n.-54_-53insT
ENST00000623417.3:c.-118+10317_-118+10318insT	ENSP00000485083.1:n.-118+10317_-118+10318...
ENST00000623517.3:c.-54_-53insT	ENSP00000485369.1:n.-54_-53insT
ENST00000624355.1:c.-215_-214insT	ENSP00000485327.1:n.-215_-214insT
ENST00000625116.3:c.-278_-277insT	ENSP00000485160.1:n.-278_-277insT
NM_001173479.1:c.-54_-53insT	NP_001166950.1:n.-54_-53insT
XM_005262249.1:c.-54_-53insT	XP_005262306.1:n.-54_-53insT
XM_005262252.1:c.-215_-214insT	XP_005262309.1:n.-215_-214insT
NM_001330495.1:c.-215_-214insT	NP_001317424.1:n.-215_-214insT
NM_001353921.1:c.-54_-53insT	NP_001340850.1:n.-54_-53insT
NM_001353922.1:c.-54_-53insT	NP_001340851.1:n.-54_-53insT
XM_017029378.2:c.-54_-53insT	XP_016884867.1:n.-54_-53insT
XM_024452358.1:c.-215_-214insT	XP_024308126.1:n.-215_-214insT
NM_001173479.2:c.-54_-53insT	NP_001166950.1:n.-54_-53insT
NM_001330495.2:c.-215_-214insT	NP_001317424.1:n.-215_-214insT
NM_001353921.2:c.-54_-53insT MANE Select	NP_001340850.1:n.-54_-53insT
NM_001353922.2:c.-54_-53insT	NP_001340851.1:n.-54_-53insT
NM_001369043.1:c.-215_-214insT	NP_001355972.1:n.-215_-214insT