Canonical Allele Identifier: CA2278712441

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868614C= , CM000679.2:g.81868614C=	GRCh38
NC_000017.10:g.79826490C= , CM000679.1:g.79826490C=	GRCh37
NC_000017.9:g.77419779C=	NCBI36
NG_034210.1:g.7793G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.*262G= MANE Select	ENSP00000269321.7:n.*262G=
ENST00000269321.11:c.*262G=	ENSP00000269321.7:n.*262G=
ENST00000400721.8:c.*262G=	ENSP00000383556.4:n.*262G=
ENST00000541078.6:c.*262G=	ENSP00000441348.2:n.*262G=
ENST00000579121.5:c.503-30G=	ENSP00000462960.1:n.503-30G=
ENST00000580685.5:c.*262G=	ENSP00000464205.1:n.*262G=
ENST00000581876.5:c.*262G=	ENSP00000461956.1:n.*262G=
ENST00000582520.1:n.17G=
ENST00000584461.5:c.503-30G=	ENSP00000463939.1:n.503-30G=
NM_001185077.2:c.*262G=	NP_001172006.1:n.*262G=
NM_001185078.2:c.*262G=	NP_001172007.1:n.*262G=
NM_001301240.1:c.503-30G=	NP_001288169.1:n.503-30G=
NM_001301241.1:c.503-30G=	NP_001288170.1:n.503-30G=
NM_001301242.1:c.765G=	NP_001288171.1:p.Gln255=
NM_001301243.1:c.*262G=	NP_001288172.1:n.*262G=
NM_004309.5:c.*262G=	NP_004300.1:n.*262G=
NR_125441.1:n.936G=
XM_011523574.1:c.*262G=	XP_011521876.1:n.*262G=
NM_004309.6:c.*262G= MANE Select	NP_004300.1:n.*262G=
NM_001185077.3:c.*262G=	NP_001172006.1:n.*262G=
NM_001185078.3:c.*262G=	NP_001172007.1:n.*262G=
NM_001301240.2:c.503-30G=	NP_001288169.1:n.503-30G=
NM_001301241.2:c.503-30G=	NP_001288170.1:n.503-30G=
NM_001301242.2:c.765G=	NP_001288171.1:p.Gln255=
NM_001301243.2:c.*262G=	NP_001288172.1:n.*262G=
NR_125441.2:n.867G=