Canonical Allele Identifier: CA2278712593
Gene: ARHGDIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868796G= , CM000679.2:g.81868796G= GRCh38
NC_000017.10:g.79826672G= , CM000679.1:g.79826672G= GRCh37
NC_000017.9:g.77419961G= NCBI36
NG_034210.1:g.7611C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.*80C= MANE Select ENSP00000269321.7:n.*80C=
ENST00000269321.11:c.*80C= ENSP00000269321.7:n.*80C=
ENST00000400721.8:c.*80C= ENSP00000383556.4:n.*80C=
ENST00000541078.6:c.*80C= ENSP00000441348.2:n.*80C=
ENST00000579121.5:c.502+193C= ENSP00000462960.1:n.502+193C=
ENST00000580685.5:c.*80C= ENSP00000464205.1:n.*80C=
ENST00000581876.5:c.*80C= ENSP00000461956.1:n.*80C=
ENST00000583868.5:c.583C= ENSP00000462209.1:p.Pro195=
ENST00000584461.5:c.502+193C= ENSP00000463939.1:n.502+193C=
NM_001185077.2:c.*80C= NP_001172006.1:n.*80C=
NM_001185078.2:c.*80C= NP_001172007.1:n.*80C=
NM_001301240.1:c.502+193C= NP_001288169.1:n.502+193C=
NM_001301241.1:c.502+193C= NP_001288170.1:n.502+193C=
NM_001301242.1:c.583C= NP_001288171.1:p.Pro195=
NM_001301243.1:c.*80C= NP_001288172.1:n.*80C=
NM_004309.5:c.*80C= NP_004300.1:n.*80C=
NR_125441.1:n.754C=
XM_011523574.1:c.*80C= XP_011521876.1:n.*80C=
NM_004309.6:c.*80C= MANE Select NP_004300.1:n.*80C=
NM_001185077.3:c.*80C= NP_001172006.1:n.*80C=
NM_001185078.3:c.*80C= NP_001172007.1:n.*80C=
NM_001301240.2:c.502+193C= NP_001288169.1:n.502+193C=
NM_001301241.2:c.502+193C= NP_001288170.1:n.502+193C=
NM_001301242.2:c.583C= NP_001288171.1:p.Pro195=
NM_001301243.2:c.*80C= NP_001288172.1:n.*80C=
NR_125441.2:n.685C=