Canonical Allele Identifier: CA2278712416

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868583_81868584delinsAC , CM000679.2:g.81868583_81868584delinsAC	GRCh38
NC_000017.10:g.79826459_79826460delinsAC , CM000679.1:g.79826459_79826460delinsAC	GRCh37
NC_000017.9:g.77419748_77419749delinsAC	NCBI36
NG_034210.1:g.7823_7824delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.*292_*293delinsGT MANE Select	ENSP00000269321.7:n.*292_*293delinsGT
ENST00000269321.11:c.*292_*293delinsGT	ENSP00000269321.7:n.*292_*293delinsGT
ENST00000400721.8:c.*292_*293delinsGT	ENSP00000383556.4:n.*292_*293delinsGT
ENST00000541078.6:c.*292_*293delinsGT	ENSP00000441348.2:n.*292_*293delinsGT
ENST00000579121.5:c.503_504delinsGT	ENSP00000462960.1:p.Gly168=
ENST00000580685.5:c.*292_*293delinsGT	ENSP00000464205.1:n.*292_*293delinsGT
ENST00000582520.1:n.46+1_46+2delinsGT
ENST00000584461.5:c.503_504delinsGT	ENSP00000463939.1:p.Gly168=
NM_001185077.2:c.*292_*293delinsGT	NP_001172006.1:n.*292_*293delinsGT
NM_001185078.2:c.*292_*293delinsGT	NP_001172007.1:n.*292_*293delinsGT
NM_001301240.1:c.503_504delinsGT	NP_001288169.1:p.Gly168=
NM_001301241.1:c.503_504delinsGT	NP_001288170.1:p.Gly168=
NM_001301242.1:c.795_796delinsGT	NP_001288171.1:p.Arg265=
NM_001301243.1:c.*292_*293delinsGT	NP_001288172.1:n.*292_*293delinsGT
NM_004309.5:c.*292_*293delinsGT	NP_004300.1:n.*292_*293delinsGT
NR_125441.1:n.966_967delinsGT
XM_011523574.1:c.*292_*293delinsGT	XP_011521876.1:n.*292_*293delinsGT
NM_004309.6:c.*292_*293delinsGT MANE Select	NP_004300.1:n.*292_*293delinsGT
NM_001185077.3:c.*292_*293delinsGT	NP_001172006.1:n.*292_*293delinsGT
NM_001185078.3:c.*292_*293delinsGT	NP_001172007.1:n.*292_*293delinsGT
NM_001301240.2:c.503_504delinsGT	NP_001288169.1:p.Gly168=
NM_001301241.2:c.503_504delinsGT	NP_001288170.1:p.Gly168=
NM_001301242.2:c.795_796delinsGT	NP_001288171.1:p.Arg265=
NM_001301243.2:c.*292_*293delinsGT	NP_001288172.1:n.*292_*293delinsGT
NR_125441.2:n.897_898delinsGT