Canonical Allele Identifier: CA8843184
Gene: ARHGDIA HGNC NCBI

Linked Data

dbSNP Id: rs760377906

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868853G>A , CM000679.2:g.81868853G>A GRCh38
NC_000017.10:g.79826729G>A , CM000679.1:g.79826729G>A GRCh37
NC_000017.9:g.77420018G>A NCBI36
NG_034210.1:g.7554C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.*23C>T MANE Select ENSP00000269321.7:n.*23C>T
ENST00000269321.11:c.*23C>T ENSP00000269321.7:n.*23C>T
ENST00000400721.8:c.*23C>T ENSP00000383556.4:n.*23C>T
ENST00000541078.6:c.*23C>T ENSP00000441348.2:n.*23C>T
ENST00000579121.5:c.502+136C>T ENSP00000462960.1:n.502+136C>T
ENST00000580685.5:c.*23C>T ENSP00000464205.1:n.*23C>T
ENST00000581876.5:c.*23C>T ENSP00000461956.1:n.*23C>T
ENST00000583868.5:c.526C>T ENSP00000462209.1:p.Gln176Ter
ENST00000584461.5:c.502+136C>T ENSP00000463939.1:n.502+136C>T
NM_001185077.2:c.*23C>T NP_001172006.1:n.*23C>T
NM_001185078.2:c.*23C>T NP_001172007.1:n.*23C>T
NM_001301240.1:c.502+136C>T NP_001288169.1:n.502+136C>T
NM_001301241.1:c.502+136C>T NP_001288170.1:n.502+136C>T
NM_001301242.1:c.526C>T NP_001288171.1:p.Gln176Ter
NM_001301243.1:c.*23C>T NP_001288172.1:n.*23C>T
NM_004309.5:c.*23C>T NP_004300.1:n.*23C>T
NR_125441.1:n.697C>T
XM_011523574.1:c.*23C>T XP_011521876.1:n.*23C>T
NM_004309.6:c.*23C>T MANE Select NP_004300.1:n.*23C>T
NM_001185077.3:c.*23C>T NP_001172006.1:n.*23C>T
NM_001185078.3:c.*23C>T NP_001172007.1:n.*23C>T
NM_001301240.2:c.502+136C>T NP_001288169.1:n.502+136C>T
NM_001301241.2:c.502+136C>T NP_001288170.1:n.502+136C>T
NM_001301242.2:c.526C>T NP_001288171.1:p.Gln176Ter
NM_001301243.2:c.*23C>T NP_001288172.1:n.*23C>T
NR_125441.2:n.628C>T