Canonical Allele Identifier: CA401523465
Gene: ARHGDIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868919G>T , CM000679.2:g.81868919G>T GRCh38
NC_000017.10:g.79826795G>T , CM000679.1:g.79826795G>T GRCh37
NC_000017.9:g.77420084G>T NCBI36
NG_034210.1:g.7488C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.572C>A MANE Select ENSP00000269321.7:p.Ser191Tyr
ENST00000269321.11:c.572C>A ENSP00000269321.7:p.Ser191Tyr
ENST00000400721.8:c.440C>A ENSP00000383556.4:p.Ser147Tyr
ENST00000541078.6:c.572C>A ENSP00000441348.2:p.Ser191Tyr
ENST00000579121.5:c.502+70C>A ENSP00000462960.1:n.502+70C>A
ENST00000580685.5:c.572C>A ENSP00000464205.1:p.Ser191Tyr
ENST00000581876.5:c.347C>A ENSP00000461956.1:p.Ser116Tyr
ENST00000582984.5:n.774C>A
ENST00000583868.5:c.460C>A ENSP00000462209.1:p.Pro154Thr
ENST00000584461.5:c.502+70C>A ENSP00000463939.1:n.502+70C>A
NM_001185077.2:c.572C>A NP_001172006.1:p.Ser191Tyr
NM_001185078.2:c.440C>A NP_001172007.1:p.Ser147Tyr
NM_001301240.1:c.502+70C>A NP_001288169.1:n.502+70C>A
NM_001301241.1:c.502+70C>A NP_001288170.1:n.502+70C>A
NM_001301242.1:c.460C>A NP_001288171.1:p.Pro154Thr
NM_001301243.1:c.707C>A NP_001288172.1:p.Ser236Tyr
NM_004309.5:c.572C>A NP_004300.1:p.Ser191Tyr
NR_125441.1:n.631C>A
XM_011523574.1:c.707C>A XP_011521876.1:p.Ser236Tyr
NM_004309.6:c.572C>A MANE Select NP_004300.1:p.Ser191Tyr
NM_001185077.3:c.572C>A NP_001172006.1:p.Ser191Tyr
NM_001185078.3:c.440C>A NP_001172007.1:p.Ser147Tyr
NM_001301240.2:c.502+70C>A NP_001288169.1:n.502+70C>A
NM_001301241.2:c.502+70C>A NP_001288170.1:n.502+70C>A
NM_001301242.2:c.460C>A NP_001288171.1:p.Pro154Thr
NM_001301243.2:c.707C>A NP_001288172.1:p.Ser236Tyr
NR_125441.2:n.562C>A