Canonical Allele Identifier: CA2504493059
Gene: ARHGDIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868799_81868804del , CM000679.2:g.81868799_81868804del GRCh38
NC_000017.10:g.79826675_79826680del , CM000679.1:g.79826675_79826680del GRCh37
NC_000017.9:g.77419964_77419969del NCBI36
NG_034210.1:g.7603_7608del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.*72_*77del MANE Select ENSP00000269321.7:n.*72_*77del
ENST00000269321.11:c.*72_*77del ENSP00000269321.7:n.*72_*77del
ENST00000400721.8:c.*72_*77del ENSP00000383556.4:n.*72_*77del
ENST00000541078.6:c.*72_*77del ENSP00000441348.2:n.*72_*77del
ENST00000579121.5:c.502+185_502+190del ENSP00000462960.1:n.502+185_502+190del
ENST00000580685.5:c.*72_*77del ENSP00000464205.1:n.*72_*77del
ENST00000581876.5:c.*72_*77del ENSP00000461956.1:n.*72_*77del
ENST00000583868.5:c.575_580del ENSP00000462209.1:p.Leu192_Ser194delinsPro
ENST00000584461.5:c.502+185_502+190del ENSP00000463939.1:n.502+185_502+190del
NM_001185077.2:c.*72_*77del NP_001172006.1:n.*72_*77del
NM_001185078.2:c.*72_*77del NP_001172007.1:n.*72_*77del
NM_001301240.1:c.502+185_502+190del NP_001288169.1:n.502+185_502+190del
NM_001301241.1:c.502+185_502+190del NP_001288170.1:n.502+185_502+190del
NM_001301242.1:c.575_580del NP_001288171.1:p.Leu192_Ser194delinsPro
NM_001301243.1:c.*72_*77del NP_001288172.1:n.*72_*77del
NM_004309.5:c.*72_*77del NP_004300.1:n.*72_*77del
NR_125441.1:n.746_751del
XM_011523574.1:c.*72_*77del XP_011521876.1:n.*72_*77del
NM_004309.6:c.*72_*77del MANE Select NP_004300.1:n.*72_*77del
NM_001185077.3:c.*72_*77del NP_001172006.1:n.*72_*77del
NM_001185078.3:c.*72_*77del NP_001172007.1:n.*72_*77del
NM_001301240.2:c.502+185_502+190del NP_001288169.1:n.502+185_502+190del
NM_001301241.2:c.502+185_502+190del NP_001288170.1:n.502+185_502+190del
NM_001301242.2:c.575_580del NP_001288171.1:p.Leu192_Ser194delinsPro
NM_001301243.2:c.*72_*77del NP_001288172.1:n.*72_*77del
NR_125441.2:n.677_682del