Canonical Allele Identifier: CA2278712500

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868684C= , CM000679.2:g.81868684C=	GRCh38
NC_000017.10:g.79826560C= , CM000679.1:g.79826560C=	GRCh37
NC_000017.9:g.77419849C=	NCBI36
NG_034210.1:g.7723G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.*192G= MANE Select	ENSP00000269321.7:n.*192G=
ENST00000269321.11:c.*192G=	ENSP00000269321.7:n.*192G=
ENST00000400721.8:c.*192G=	ENSP00000383556.4:n.*192G=
ENST00000541078.6:c.*192G=	ENSP00000441348.2:n.*192G=
ENST00000579121.5:c.503-100G=	ENSP00000462960.1:n.503-100G=
ENST00000580685.5:c.*192G=	ENSP00000464205.1:n.*192G=
ENST00000581876.5:c.*192G=	ENSP00000461956.1:n.*192G=
ENST00000583868.5:c.695G=	ENSP00000462209.1:p.Gly232=
ENST00000584461.5:c.503-100G=	ENSP00000463939.1:n.503-100G=
NM_001185077.2:c.*192G=	NP_001172006.1:n.*192G=
NM_001185078.2:c.*192G=	NP_001172007.1:n.*192G=
NM_001301240.1:c.503-100G=	NP_001288169.1:n.503-100G=
NM_001301241.1:c.503-100G=	NP_001288170.1:n.503-100G=
NM_001301242.1:c.695G=	NP_001288171.1:p.Gly232=
NM_001301243.1:c.*192G=	NP_001288172.1:n.*192G=
NM_004309.5:c.*192G=	NP_004300.1:n.*192G=
NR_125441.1:n.866G=
XM_011523574.1:c.*192G=	XP_011521876.1:n.*192G=
NM_004309.6:c.*192G= MANE Select	NP_004300.1:n.*192G=
NM_001185077.3:c.*192G=	NP_001172006.1:n.*192G=
NM_001185078.3:c.*192G=	NP_001172007.1:n.*192G=
NM_001301240.2:c.503-100G=	NP_001288169.1:n.503-100G=
NM_001301241.2:c.503-100G=	NP_001288170.1:n.503-100G=
NM_001301242.2:c.695G=	NP_001288171.1:p.Gly232=
NM_001301243.2:c.*192G=	NP_001288172.1:n.*192G=
NR_125441.2:n.797G=