Canonical Allele Identifier: CA163432
Gene: ARHGDIA HGNC NCBI

Linked Data

ClinVar Variation Id: 140594
ClinVar RCV Id: RCV000128809
dbSNP Id: rs587777553

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81869230G>A , CM000679.2:g.81869230G>A GRCh38
NC_000017.10:g.79827106G>A , CM000679.1:g.79827106G>A GRCh37
NC_000017.9:g.77420395G>A NCBI36
NG_034210.1:g.7177C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000269321.12:c.358C>T MANE Select ENSP00000269321.7:p.Arg120Ter
ENST00000269321.11:c.358C>T ENSP00000269321.7:p.Arg120Ter
ENST00000400721.8:c.358C>T ENSP00000383556.4:p.Arg120Ter
ENST00000541078.6:c.358C>T ENSP00000441348.2:p.Arg120Ter
ENST00000578351.1:c.*2C>T
ENST00000579121.5:c.358C>T ENSP00000462960.1:p.Arg120Ter
ENST00000580033.5:c.*2C>T
ENST00000580685.5:c.358C>T ENSP00000464205.1:p.Arg120Ter
ENST00000581876.5:c.191-155C>T ENSP00000461956.1:p.=
ENST00000582984.5:n.560C>T
ENST00000583111.5:n.510C>T
ENST00000583791.1:n.222C>T
ENST00000583868.5:c.358C>T ENSP00000462209.1:p.Arg120Ter
ENST00000584461.5:c.358C>T ENSP00000463939.1:p.Arg120Ter
NM_001185077.2:c.358C>T NP_001172006.1:p.Arg120Ter
NM_001185078.2:c.358C>T NP_001172007.1:p.Arg120Ter
NM_001301240.1:c.358C>T NP_001288169.1:p.Arg120Ter
NM_001301241.1:c.358C>T NP_001288170.1:p.Arg120Ter
NM_001301242.1:c.358C>T NP_001288171.1:p.Arg120Ter
NM_001301243.1:c.493C>T NP_001288172.1:p.Arg165Ter
NM_004309.5:c.358C>T NP_004300.1:p.Arg120Ter
NR_125441.1:n.417C>T
XM_011523574.1:c.493C>T XP_011521876.1:p.Arg165Ter
NM_004309.6:c.358C>T MANE Select NP_004300.1:p.Arg120Ter
NM_001185077.3:c.358C>T NP_001172006.1:p.Arg120Ter
NM_001185078.3:c.358C>T NP_001172007.1:p.Arg120Ter
NM_001301240.2:c.358C>T NP_001288169.1:p.Arg120Ter
NM_001301241.2:c.358C>T NP_001288170.1:p.Arg120Ter
NM_001301242.2:c.358C>T NP_001288171.1:p.Arg120Ter
NM_001301243.2:c.493C>T NP_001288172.1:p.Arg165Ter
NR_125441.2:n.348C>T