Canonical Allele Identifier: CA2278712850

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869220A= , CM000679.2:g.81869220A=	GRCh38
NC_000017.10:g.79827096A= , CM000679.1:g.79827096A=	GRCh37
NC_000017.9:g.77420385A=	NCBI36
NG_034210.1:g.7187T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.368T= MANE Select	ENSP00000269321.7:p.Val123=
ENST00000269321.11:c.368T=	ENSP00000269321.7:p.Val123=
ENST00000400721.8:c.368T=	ENSP00000383556.4:p.Val123=
ENST00000541078.6:c.368T=	ENSP00000441348.2:p.Val123=
ENST00000578351.1:c.*12T=	ENSP00000462323.1:n.*12T=
ENST00000579121.5:c.368T=	ENSP00000462960.1:p.Val123=
ENST00000580033.5:c.*12T=	ENSP00000463530.1:n.*12T=
ENST00000580685.5:c.368T=	ENSP00000464205.1:p.Val123=
ENST00000581876.5:c.191-145T=	ENSP00000461956.1:n.191-145T=
ENST00000582984.5:n.570T=
ENST00000583111.5:n.520T=
ENST00000583791.1:n.232T=
ENST00000583868.5:c.368T=	ENSP00000462209.1:p.Val123=
ENST00000584461.5:c.368T=	ENSP00000463939.1:p.Val123=
NM_001185077.2:c.368T=	NP_001172006.1:p.Val123=
NM_001185078.2:c.368T=	NP_001172007.1:p.Val123=
NM_001301240.1:c.368T=	NP_001288169.1:p.Val123=
NM_001301241.1:c.368T=	NP_001288170.1:p.Val123=
NM_001301242.1:c.368T=	NP_001288171.1:p.Val123=
NM_001301243.1:c.503T=	NP_001288172.1:p.Val168=
NM_004309.5:c.368T=	NP_004300.1:p.Val123=
NR_125441.1:n.427T=
XM_011523574.1:c.503T=	XP_011521876.1:p.Val168=
NM_004309.6:c.368T= MANE Select	NP_004300.1:p.Val123=
NM_001185077.3:c.368T=	NP_001172006.1:p.Val123=
NM_001185078.3:c.368T=	NP_001172007.1:p.Val123=
NM_001301240.2:c.368T=	NP_001288169.1:p.Val123=
NM_001301241.2:c.368T=	NP_001288170.1:p.Val123=
NM_001301242.2:c.368T=	NP_001288171.1:p.Val123=
NM_001301243.2:c.503T=	NP_001288172.1:p.Val168=
NR_125441.2:n.358T=