Canonical Allele Identifier: CA2278712748
Gene: ARHGDIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81869048C= , CM000679.2:g.81869048C= GRCh38
NC_000017.10:g.79826924C= , CM000679.1:g.79826924C= GRCh37
NC_000017.9:g.77420213C= NCBI36
NG_034210.1:g.7359G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.443G= MANE Select ENSP00000269321.7:p.Ser148=
ENST00000269321.11:c.443G= ENSP00000269321.7:p.Ser148=
ENST00000400721.8:c.416-105G= ENSP00000383556.4:n.416-105G=
ENST00000541078.6:c.443G= ENSP00000441348.2:p.Ser148=
ENST00000579121.5:c.443G= ENSP00000462960.1:p.Ser148=
ENST00000580033.5:c.*87G= ENSP00000463530.1:n.*87G=
ENST00000580685.5:c.443G= ENSP00000464205.1:p.Ser148=
ENST00000581876.5:c.218G= ENSP00000461956.1:p.Ser73=
ENST00000582984.5:n.645G=
ENST00000583791.1:n.307G=
ENST00000583868.5:c.435+8G= ENSP00000462209.1:n.435+8G=
ENST00000584461.5:c.443G= ENSP00000463939.1:p.Ser148=
NM_001185077.2:c.443G= NP_001172006.1:p.Ser148=
NM_001185078.2:c.416-105G= NP_001172007.1:n.416-105G=
NM_001301240.1:c.443G= NP_001288169.1:p.Ser148=
NM_001301241.1:c.443G= NP_001288170.1:p.Ser148=
NM_001301242.1:c.435+8G= NP_001288171.1:n.435+8G=
NM_001301243.1:c.578G= NP_001288172.1:p.Ser193=
NM_004309.5:c.443G= NP_004300.1:p.Ser148=
NR_125441.1:n.502G=
XM_011523574.1:c.578G= XP_011521876.1:p.Ser193=
NM_004309.6:c.443G= MANE Select NP_004300.1:p.Ser148=
NM_001185077.3:c.443G= NP_001172006.1:p.Ser148=
NM_001185078.3:c.416-105G= NP_001172007.1:n.416-105G=
NM_001301240.2:c.443G= NP_001288169.1:p.Ser148=
NM_001301241.2:c.443G= NP_001288170.1:p.Ser148=
NM_001301242.2:c.435+8G= NP_001288171.1:n.435+8G=
NM_001301243.2:c.578G= NP_001288172.1:p.Ser193=
NR_125441.2:n.433G=