Canonical Allele Identifier: CA2838706579
Gene: ARHGDIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81869040del , CM000679.2:g.81869040del GRCh38
NC_000017.10:g.79826916del , CM000679.1:g.79826916del GRCh37
NC_000017.9:g.77420205del NCBI36
NG_034210.1:g.7370del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.454del MANE Select ENSP00000269321.7:p.Arg152GlyfsTer8
ENST00000269321.11:c.454del ENSP00000269321.7:p.Arg152GlyfsTer8
ENST00000400721.8:c.416-94del ENSP00000383556.4:n.416-94del
ENST00000541078.6:c.454del ENSP00000441348.2:p.Arg152GlyfsTer8
ENST00000579121.5:c.454del ENSP00000462960.1:p.Arg152GlyfsTer8
ENST00000580033.5:c.*98del ENSP00000463530.1:n.*98del
ENST00000580685.5:c.454del ENSP00000464205.1:p.Arg152GlyfsTer8
ENST00000581876.5:c.229del ENSP00000461956.1:p.Arg77GlyfsTer8
ENST00000582984.5:n.656del
ENST00000583791.1:n.318del
ENST00000583868.5:c.435+19del ENSP00000462209.1:n.435+19del
ENST00000584461.5:c.454del ENSP00000463939.1:p.Arg152GlyfsTer8
NM_001185077.2:c.454del NP_001172006.1:p.Arg152GlyfsTer8
NM_001185078.2:c.416-94del NP_001172007.1:n.416-94del
NM_001301240.1:c.454del NP_001288169.1:p.Arg152GlyfsTer8
NM_001301241.1:c.454del NP_001288170.1:p.Arg152GlyfsTer8
NM_001301242.1:c.435+19del NP_001288171.1:n.435+19del
NM_001301243.1:c.589del NP_001288172.1:p.Arg197GlyfsTer8
NM_004309.5:c.454del NP_004300.1:p.Arg152GlyfsTer8
NR_125441.1:n.513del
XM_011523574.1:c.589del XP_011521876.1:p.Arg197GlyfsTer8
NM_004309.6:c.454del MANE Select NP_004300.1:p.Arg152GlyfsTer8
NM_001185077.3:c.454del NP_001172006.1:p.Arg152GlyfsTer8
NM_001185078.3:c.416-94del NP_001172007.1:n.416-94del
NM_001301240.2:c.454del NP_001288169.1:p.Arg152GlyfsTer8
NM_001301241.2:c.454del NP_001288170.1:p.Arg152GlyfsTer8
NM_001301242.2:c.435+19del NP_001288171.1:n.435+19del
NM_001301243.2:c.589del NP_001288172.1:p.Arg197GlyfsTer8
NR_125441.2:n.444del