Canonical Allele Identifier: CA2576427315
Gene: ARHGDIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868657dup , CM000679.2:g.81868657dup GRCh38
NC_000017.10:g.79826533dup , CM000679.1:g.79826533dup GRCh37
NC_000017.9:g.77419822dup NCBI36
NG_034210.1:g.7751dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.*220dup MANE Select ENSP00000269321.7:n.*220dup
ENST00000269321.11:c.*220dup ENSP00000269321.7:n.*220dup
ENST00000400721.8:c.*220dup ENSP00000383556.4:n.*220dup
ENST00000541078.6:c.*220dup ENSP00000441348.2:n.*220dup
ENST00000579121.5:c.503-72dup ENSP00000462960.1:n.503-72dup
ENST00000580685.5:c.*220dup ENSP00000464205.1:n.*220dup
ENST00000581876.5:c.*220dup ENSP00000461956.1:n.*220dup
ENST00000583868.5:c.723dup ENSP00000462209.1:p.Ala242CysfsTer?
ENST00000584461.5:c.503-72dup ENSP00000463939.1:n.503-72dup
NM_001185077.2:c.*220dup NP_001172006.1:n.*220dup
NM_001185078.2:c.*220dup NP_001172007.1:n.*220dup
NM_001301240.1:c.503-72dup NP_001288169.1:n.503-72dup
NM_001301241.1:c.503-72dup NP_001288170.1:n.503-72dup
NM_001301242.1:c.723dup NP_001288171.1:p.Ala242CysfsTer?
NM_001301243.1:c.*220dup NP_001288172.1:n.*220dup
NM_004309.5:c.*220dup NP_004300.1:n.*220dup
NR_125441.1:n.894dup
XM_011523574.1:c.*220dup XP_011521876.1:n.*220dup
NM_004309.6:c.*220dup MANE Select NP_004300.1:n.*220dup
NM_001185077.3:c.*220dup NP_001172006.1:n.*220dup
NM_001185078.3:c.*220dup NP_001172007.1:n.*220dup
NM_001301240.2:c.503-72dup NP_001288169.1:n.503-72dup
NM_001301241.2:c.503-72dup NP_001288170.1:n.503-72dup
NM_001301242.2:c.723dup NP_001288171.1:p.Ala242CysfsTer?
NM_001301243.2:c.*220dup NP_001288172.1:n.*220dup
NR_125441.2:n.825dup