Canonical Allele Identifier: CA2810643531

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869308G>T , CM000679.2:g.81869308G>T	GRCh38
NC_000017.10:g.79827184G>T , CM000679.1:g.79827184G>T	GRCh37
NC_000017.9:g.77420473G>T	NCBI36
NG_034210.1:g.7099C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.351+22C>A MANE Select	ENSP00000269321.7:n.351+22C>A
ENST00000269321.11:c.351+22C>A	ENSP00000269321.7:n.351+22C>A
ENST00000400721.8:c.351+22C>A	ENSP00000383556.4:n.351+22C>A
ENST00000541078.6:c.351+22C>A	ENSP00000441348.2:n.351+22C>A
ENST00000578351.1:c.275-72C>A	ENSP00000462323.1:n.275-72C>A
ENST00000579121.5:c.351+22C>A	ENSP00000462960.1:n.351+22C>A
ENST00000580033.5:c.275-72C>A	ENSP00000463530.1:n.275-72C>A
ENST00000580685.5:c.351+22C>A	ENSP00000464205.1:n.351+22C>A
ENST00000581876.5:c.191-233C>A	ENSP00000461956.1:n.191-233C>A
ENST00000582984.5:n.553+22C>A
ENST00000583111.5:n.432C>A
ENST00000583791.1:n.144C>A
ENST00000583868.5:c.351+22C>A	ENSP00000462209.1:n.351+22C>A
ENST00000584397.1:n.616C>A
ENST00000584461.5:c.351+22C>A	ENSP00000463939.1:n.351+22C>A
NM_001185077.2:c.351+22C>A	NP_001172006.1:n.351+22C>A
NM_001185078.2:c.351+22C>A	NP_001172007.1:n.351+22C>A
NM_001301240.1:c.351+22C>A	NP_001288169.1:n.351+22C>A
NM_001301241.1:c.351+22C>A	NP_001288170.1:n.351+22C>A
NM_001301242.1:c.351+22C>A	NP_001288171.1:n.351+22C>A
NM_001301243.1:c.486+22C>A	NP_001288172.1:n.486+22C>A
NM_004309.5:c.351+22C>A	NP_004300.1:n.351+22C>A
NR_125441.1:n.411-72C>A
XM_011523574.1:c.486+22C>A	XP_011521876.1:n.486+22C>A
NM_004309.6:c.351+22C>A MANE Select	NP_004300.1:n.351+22C>A
NM_001185077.3:c.351+22C>A	NP_001172006.1:n.351+22C>A
NM_001185078.3:c.351+22C>A	NP_001172007.1:n.351+22C>A
NM_001301240.2:c.351+22C>A	NP_001288169.1:n.351+22C>A
NM_001301241.2:c.351+22C>A	NP_001288170.1:n.351+22C>A
NM_001301242.2:c.351+22C>A	NP_001288171.1:n.351+22C>A
NM_001301243.2:c.486+22C>A	NP_001288172.1:n.486+22C>A
NR_125441.2:n.342-72C>A