Canonical Allele Identifier: CA401523174
Gene: ARHGDIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868880T>C , CM000679.2:g.81868880T>C GRCh38
NC_000017.10:g.79826756T>C , CM000679.1:g.79826756T>C GRCh37
NC_000017.9:g.77420045T>C NCBI36
NG_034210.1:g.7527A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.611A>G MANE Select ENSP00000269321.7:p.Asp204Gly
ENST00000269321.11:c.611A>G ENSP00000269321.7:p.Asp204Gly
ENST00000400721.8:c.479A>G ENSP00000383556.4:p.Asp160Gly
ENST00000541078.6:c.611A>G ENSP00000441348.2:p.Asp204Gly
ENST00000579121.5:c.502+109A>G ENSP00000462960.1:n.502+109A>G
ENST00000580685.5:c.611A>G ENSP00000464205.1:p.Asp204Gly
ENST00000581876.5:c.386A>G ENSP00000461956.1:p.Asp129Gly
ENST00000582984.5:n.813A>G
ENST00000583868.5:c.499A>G ENSP00000462209.1:p.Thr167Ala
ENST00000584461.5:c.502+109A>G ENSP00000463939.1:n.502+109A>G
NM_001185077.2:c.611A>G NP_001172006.1:p.Asp204Gly
NM_001185078.2:c.479A>G NP_001172007.1:p.Asp160Gly
NM_001301240.1:c.502+109A>G NP_001288169.1:n.502+109A>G
NM_001301241.1:c.502+109A>G NP_001288170.1:n.502+109A>G
NM_001301242.1:c.499A>G NP_001288171.1:p.Thr167Ala
NM_001301243.1:c.746A>G NP_001288172.1:p.Asp249Gly
NM_004309.5:c.611A>G NP_004300.1:p.Asp204Gly
NR_125441.1:n.670A>G
XM_011523574.1:c.746A>G XP_011521876.1:p.Asp249Gly
NM_004309.6:c.611A>G MANE Select NP_004300.1:p.Asp204Gly
NM_001185077.3:c.611A>G NP_001172006.1:p.Asp204Gly
NM_001185078.3:c.479A>G NP_001172007.1:p.Asp160Gly
NM_001301240.2:c.502+109A>G NP_001288169.1:n.502+109A>G
NM_001301241.2:c.502+109A>G NP_001288170.1:n.502+109A>G
NM_001301242.2:c.499A>G NP_001288171.1:p.Thr167Ala
NM_001301243.2:c.746A>G NP_001288172.1:p.Asp249Gly
NR_125441.2:n.601A>G