Canonical Allele Identifier: CA2278712691

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868930G= , CM000679.2:g.81868930G=	GRCh38
NC_000017.10:g.79826806G= , CM000679.1:g.79826806G=	GRCh37
NC_000017.9:g.77420095G=	NCBI36
NG_034210.1:g.7477C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.561C= MANE Select	ENSP00000269321.7:p.Thr187=
ENST00000269321.11:c.561C=	ENSP00000269321.7:p.Thr187=
ENST00000400721.8:c.429C=	ENSP00000383556.4:p.Thr143=
ENST00000541078.6:c.561C=	ENSP00000441348.2:p.Thr187=
ENST00000579121.5:c.502+59C=	ENSP00000462960.1:n.502+59C=
ENST00000580033.5:c.*205C=	ENSP00000463530.1:n.*205C=
ENST00000580685.5:c.561C=	ENSP00000464205.1:p.Thr187=
ENST00000581876.5:c.336C=	ENSP00000461956.1:p.Thr112=
ENST00000582984.5:n.763C=
ENST00000583868.5:c.449C=	ENSP00000462209.1:p.Pro150=
ENST00000584461.5:c.502+59C=	ENSP00000463939.1:n.502+59C=
NM_001185077.2:c.561C=	NP_001172006.1:p.Thr187=
NM_001185078.2:c.429C=	NP_001172007.1:p.Thr143=
NM_001301240.1:c.502+59C=	NP_001288169.1:n.502+59C=
NM_001301241.1:c.502+59C=	NP_001288170.1:n.502+59C=
NM_001301242.1:c.449C=	NP_001288171.1:p.Pro150=
NM_001301243.1:c.696C=	NP_001288172.1:p.Thr232=
NM_004309.5:c.561C=	NP_004300.1:p.Thr187=
NR_125441.1:n.620C=
XM_011523574.1:c.696C=	XP_011521876.1:p.Thr232=
NM_004309.6:c.561C= MANE Select	NP_004300.1:p.Thr187=
NM_001185077.3:c.561C=	NP_001172006.1:p.Thr187=
NM_001185078.3:c.429C=	NP_001172007.1:p.Thr143=
NM_001301240.2:c.502+59C=	NP_001288169.1:n.502+59C=
NM_001301241.2:c.502+59C=	NP_001288170.1:n.502+59C=
NM_001301242.2:c.449C=	NP_001288171.1:p.Pro150=
NM_001301243.2:c.696C=	NP_001288172.1:p.Thr232=
NR_125441.2:n.551C=