Canonical Allele Identifier: CA986872806
Gene: ARHGDIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868751_81868811del , CM000679.2:g.81868751_81868811del GRCh38
NC_000017.10:g.79826627_79826687del , CM000679.1:g.79826627_79826687del GRCh37
NC_000017.9:g.77419916_77419976del NCBI36
NG_034210.1:g.7597_7657del

Transcript Alleles

HGVS Amino-acid change
ENST00000269321.12:c.*66_*126del MANE Select ENSP00000269321.7:n.*66_*126del
ENST00000269321.11:c.*66_*126del ENSP00000269321.7:n.*66_*126del
ENST00000400721.8:c.*66_*126del ENSP00000383556.4:n.*66_*126del
ENST00000541078.6:c.*66_*126del ENSP00000441348.2:n.*66_*126del
ENST00000579121.5:c.502+179_503-166del ENSP00000462960.1:n.502+179_503-166del
ENST00000580685.5:c.*66_*126del ENSP00000464205.1:n.*66_*126del
ENST00000581876.5:c.*66_*126del ENSP00000461956.1:n.*66_*126del
ENST00000583868.5:c.569_629del ENSP00000462209.1:p.Gln190ProfsTer?
ENST00000584461.5:c.502+179_503-166del ENSP00000463939.1:n.502+179_503-166del
NM_001185077.2:c.*66_*126del NP_001172006.1:n.*66_*126del
NM_001185078.2:c.*66_*126del NP_001172007.1:n.*66_*126del
NM_001301240.1:c.502+179_503-166del NP_001288169.1:n.502+179_503-166del
NM_001301241.1:c.502+179_503-166del NP_001288170.1:n.502+179_503-166del
NM_001301242.1:c.569_629del NP_001288171.1:p.Gln190ProfsTer?
NM_001301243.1:c.*66_*126del NP_001288172.1:n.*66_*126del
NM_004309.5:c.*66_*126del NP_004300.1:n.*66_*126del
NR_125441.1:n.740_800del
XM_011523574.1:c.*66_*126del XP_011521876.1:n.*66_*126del
NM_004309.6:c.*66_*126del MANE Select NP_004300.1:n.*66_*126del
NM_001185077.3:c.*66_*126del NP_001172006.1:n.*66_*126del
NM_001185078.3:c.*66_*126del NP_001172007.1:n.*66_*126del
NM_001301240.2:c.502+179_503-166del NP_001288169.1:n.502+179_503-166del
NM_001301241.2:c.502+179_503-166del NP_001288170.1:n.502+179_503-166del
NM_001301242.2:c.569_629del NP_001288171.1:p.Gln190ProfsTer?
NM_001301243.2:c.*66_*126del NP_001288172.1:n.*66_*126del
NR_125441.2:n.671_731del