Canonical Allele Identifier: CA2278712673

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868890C= , CM000679.2:g.81868890C=	GRCh38
NC_000017.10:g.79826766C= , CM000679.1:g.79826766C=	GRCh37
NC_000017.9:g.77420055C=	NCBI36
NG_034210.1:g.7517G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.601G= MANE Select	ENSP00000269321.7:p.Asp201=
ENST00000269321.11:c.601G=	ENSP00000269321.7:p.Asp201=
ENST00000400721.8:c.469G=	ENSP00000383556.4:p.Asp157=
ENST00000541078.6:c.601G=	ENSP00000441348.2:p.Asp201=
ENST00000579121.5:c.502+99G=	ENSP00000462960.1:n.502+99G=
ENST00000580685.5:c.601G=	ENSP00000464205.1:p.Asp201=
ENST00000581876.5:c.376G=	ENSP00000461956.1:p.Asp126=
ENST00000582984.5:n.803G=
ENST00000583868.5:c.489G=	ENSP00000462209.1:p.Arg163=
ENST00000584461.5:c.502+99G=	ENSP00000463939.1:n.502+99G=
NM_001185077.2:c.601G=	NP_001172006.1:p.Asp201=
NM_001185078.2:c.469G=	NP_001172007.1:p.Asp157=
NM_001301240.1:c.502+99G=	NP_001288169.1:n.502+99G=
NM_001301241.1:c.502+99G=	NP_001288170.1:n.502+99G=
NM_001301242.1:c.489G=	NP_001288171.1:p.Arg163=
NM_001301243.1:c.736G=	NP_001288172.1:p.Asp246=
NM_004309.5:c.601G=	NP_004300.1:p.Asp201=
NR_125441.1:n.660G=
XM_011523574.1:c.736G=	XP_011521876.1:p.Asp246=
NM_004309.6:c.601G= MANE Select	NP_004300.1:p.Asp201=
NM_001185077.3:c.601G=	NP_001172006.1:p.Asp201=
NM_001185078.3:c.469G=	NP_001172007.1:p.Asp157=
NM_001301240.2:c.502+99G=	NP_001288169.1:n.502+99G=
NM_001301241.2:c.502+99G=	NP_001288170.1:n.502+99G=
NM_001301242.2:c.489G=	NP_001288171.1:p.Arg163=
NM_001301243.2:c.736G=	NP_001288172.1:p.Asp246=
NR_125441.2:n.591G=