Canonical Allele Identifier: CA8843223
Gene: ARHGDIA HGNC NCBI

Linked Data

dbSNP Id: rs150457411

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81869028C>T , CM000679.2:g.81869028C>T GRCh38
NC_000017.10:g.79826904C>T , CM000679.1:g.79826904C>T GRCh37
NC_000017.9:g.77420193C>T NCBI36
NG_034210.1:g.7379G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.463G>A MANE Select ENSP00000269321.7:p.Glu155Lys
ENST00000269321.11:c.463G>A ENSP00000269321.7:p.Glu155Lys
ENST00000400721.8:c.416-85G>A ENSP00000383556.4:n.416-85G>A
ENST00000541078.6:c.463G>A ENSP00000441348.2:p.Glu155Lys
ENST00000579121.5:c.463G>A ENSP00000462960.1:p.Glu155Lys
ENST00000580033.5:c.*107G>A ENSP00000463530.1:n.*107G>A
ENST00000580685.5:c.463G>A ENSP00000464205.1:p.Glu155Lys
ENST00000581876.5:c.238G>A ENSP00000461956.1:p.Glu80Lys
ENST00000582984.5:n.665G>A
ENST00000583791.1:n.327G>A
ENST00000583868.5:c.435+28G>A ENSP00000462209.1:n.435+28G>A
ENST00000584461.5:c.463G>A ENSP00000463939.1:p.Glu155Lys
NM_001185077.2:c.463G>A NP_001172006.1:p.Glu155Lys
NM_001185078.2:c.416-85G>A NP_001172007.1:n.416-85G>A
NM_001301240.1:c.463G>A NP_001288169.1:p.Glu155Lys
NM_001301241.1:c.463G>A NP_001288170.1:p.Glu155Lys
NM_001301242.1:c.435+28G>A NP_001288171.1:n.435+28G>A
NM_001301243.1:c.598G>A NP_001288172.1:p.Glu200Lys
NM_004309.5:c.463G>A NP_004300.1:p.Glu155Lys
NR_125441.1:n.522G>A
XM_011523574.1:c.598G>A XP_011521876.1:p.Glu200Lys
NM_004309.6:c.463G>A MANE Select NP_004300.1:p.Glu155Lys
NM_001185077.3:c.463G>A NP_001172006.1:p.Glu155Lys
NM_001185078.3:c.416-85G>A NP_001172007.1:n.416-85G>A
NM_001301240.2:c.463G>A NP_001288169.1:p.Glu155Lys
NM_001301241.2:c.463G>A NP_001288170.1:p.Glu155Lys
NM_001301242.2:c.435+28G>A NP_001288171.1:n.435+28G>A
NM_001301243.2:c.598G>A NP_001288172.1:p.Glu200Lys
NR_125441.2:n.453G>A