Canonical Allele Identifier: CA2278712738

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869032G= , CM000679.2:g.81869032G=	GRCh38
NC_000017.10:g.79826908G= , CM000679.1:g.79826908G=	GRCh37
NC_000017.9:g.77420197G=	NCBI36
NG_034210.1:g.7375C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.459C= MANE Select	ENSP00000269321.7:p.Ala153=
ENST00000269321.11:c.459C=	ENSP00000269321.7:p.Ala153=
ENST00000400721.8:c.416-89C=	ENSP00000383556.4:n.416-89C=
ENST00000541078.6:c.459C=	ENSP00000441348.2:p.Ala153=
ENST00000579121.5:c.459C=	ENSP00000462960.1:p.Ala153=
ENST00000580033.5:c.*103C=	ENSP00000463530.1:n.*103C=
ENST00000580685.5:c.459C=	ENSP00000464205.1:p.Ala153=
ENST00000581876.5:c.234C=	ENSP00000461956.1:p.Ala78=
ENST00000582984.5:n.661C=
ENST00000583791.1:n.323C=
ENST00000583868.5:c.435+24C=	ENSP00000462209.1:n.435+24C=
ENST00000584461.5:c.459C=	ENSP00000463939.1:p.Ala153=
NM_001185077.2:c.459C=	NP_001172006.1:p.Ala153=
NM_001185078.2:c.416-89C=	NP_001172007.1:n.416-89C=
NM_001301240.1:c.459C=	NP_001288169.1:p.Ala153=
NM_001301241.1:c.459C=	NP_001288170.1:p.Ala153=
NM_001301242.1:c.435+24C=	NP_001288171.1:n.435+24C=
NM_001301243.1:c.594C=	NP_001288172.1:p.Ala198=
NM_004309.5:c.459C=	NP_004300.1:p.Ala153=
NR_125441.1:n.518C=
XM_011523574.1:c.594C=	XP_011521876.1:p.Ala198=
NM_004309.6:c.459C= MANE Select	NP_004300.1:p.Ala153=
NM_001185077.3:c.459C=	NP_001172006.1:p.Ala153=
NM_001185078.3:c.416-89C=	NP_001172007.1:n.416-89C=
NM_001301240.2:c.459C=	NP_001288169.1:p.Ala153=
NM_001301241.2:c.459C=	NP_001288170.1:p.Ala153=
NM_001301242.2:c.435+24C=	NP_001288171.1:n.435+24C=
NM_001301243.2:c.594C=	NP_001288172.1:p.Ala198=
NR_125441.2:n.449C=