Canonical Allele Identifier: CA645599654
Gene: ARHGDIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81869012del , CM000679.2:g.81869012del GRCh38
NC_000017.10:g.79826888del , CM000679.1:g.79826888del GRCh37
NC_000017.9:g.77420177del NCBI36
NG_034210.1:g.7399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.483del MANE Select ENSP00000269321.7:p.Val162TrpfsTer?
ENST00000269321.11:c.483del ENSP00000269321.7:p.Val162TrpfsTer?
ENST00000400721.8:c.416-65del ENSP00000383556.4:n.416-65del
ENST00000541078.6:c.483del ENSP00000441348.2:p.Val162TrpfsTer?
ENST00000579121.5:c.483del ENSP00000462960.1:p.Val162TrpfsTer?
ENST00000580033.5:c.*127del ENSP00000463530.1:n.*127del
ENST00000580685.5:c.483del ENSP00000464205.1:p.Val162TrpfsTer?
ENST00000581876.5:c.258del ENSP00000461956.1:p.Val87TrpfsTer?
ENST00000582984.5:n.685del
ENST00000583791.1:n.347del
ENST00000583868.5:c.435+48del ENSP00000462209.1:n.435+48del
ENST00000584461.5:c.483del ENSP00000463939.1:p.Val162TrpfsTer?
NM_001185077.2:c.483del NP_001172006.1:p.Val162TrpfsTer?
NM_001185078.2:c.416-65del NP_001172007.1:n.416-65del
NM_001301240.1:c.483del NP_001288169.1:p.Val162TrpfsTer?
NM_001301241.1:c.483del NP_001288170.1:p.Val162TrpfsTer?
NM_001301242.1:c.435+48del NP_001288171.1:n.435+48del
NM_001301243.1:c.618del NP_001288172.1:p.Val207TrpfsTer?
NM_004309.5:c.483del NP_004300.1:p.Val162TrpfsTer?
NR_125441.1:n.542del
XM_011523574.1:c.618del XP_011521876.1:p.Val207TrpfsTer?
NM_004309.6:c.483del MANE Select NP_004300.1:p.Val162TrpfsTer?
NM_001185077.3:c.483del NP_001172006.1:p.Val162TrpfsTer?
NM_001185078.3:c.416-65del NP_001172007.1:n.416-65del
NM_001301240.2:c.483del NP_001288169.1:p.Val162TrpfsTer?
NM_001301241.2:c.483del NP_001288170.1:p.Val162TrpfsTer?
NM_001301242.2:c.435+48del NP_001288171.1:n.435+48del
NM_001301243.2:c.618del NP_001288172.1:p.Val207TrpfsTer?
NR_125441.2:n.473del