Canonical Allele Identifier: CA8843215
Gene: ARHGDIA HGNC NCBI

Linked Data

dbSNP Id: rs756496364

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81869011G>A , CM000679.2:g.81869011G>A GRCh38
NC_000017.10:g.79826887G>A , CM000679.1:g.79826887G>A GRCh37
NC_000017.9:g.77420176G>A NCBI36
NG_034210.1:g.7396C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.480C>T MANE Select ENSP00000269321.7:p.Thr160=
ENST00000269321.11:c.480C>T ENSP00000269321.7:p.Thr160=
ENST00000400721.8:c.416-68C>T ENSP00000383556.4:n.416-68C>T
ENST00000541078.6:c.480C>T ENSP00000441348.2:p.Thr160=
ENST00000579121.5:c.480C>T ENSP00000462960.1:p.Thr160=
ENST00000580033.5:c.*124C>T ENSP00000463530.1:n.*124C>T
ENST00000580685.5:c.480C>T ENSP00000464205.1:p.Thr160=
ENST00000581876.5:c.255C>T ENSP00000461956.1:p.Thr85=
ENST00000582984.5:n.682C>T
ENST00000583791.1:n.344C>T
ENST00000583868.5:c.435+45C>T ENSP00000462209.1:n.435+45C>T
ENST00000584461.5:c.480C>T ENSP00000463939.1:p.Thr160=
NM_001185077.2:c.480C>T NP_001172006.1:p.Thr160=
NM_001185078.2:c.416-68C>T NP_001172007.1:n.416-68C>T
NM_001301240.1:c.480C>T NP_001288169.1:p.Thr160=
NM_001301241.1:c.480C>T NP_001288170.1:p.Thr160=
NM_001301242.1:c.435+45C>T NP_001288171.1:n.435+45C>T
NM_001301243.1:c.615C>T NP_001288172.1:p.Thr205=
NM_004309.5:c.480C>T NP_004300.1:p.Thr160=
NR_125441.1:n.539C>T
XM_011523574.1:c.615C>T XP_011521876.1:p.Thr205=
NM_004309.6:c.480C>T MANE Select NP_004300.1:p.Thr160=
NM_001185077.3:c.480C>T NP_001172006.1:p.Thr160=
NM_001185078.3:c.416-68C>T NP_001172007.1:n.416-68C>T
NM_001301240.2:c.480C>T NP_001288169.1:p.Thr160=
NM_001301241.2:c.480C>T NP_001288170.1:p.Thr160=
NM_001301242.2:c.435+45C>T NP_001288171.1:n.435+45C>T
NM_001301243.2:c.615C>T NP_001288172.1:p.Thr205=
NR_125441.2:n.470C>T