Canonical Allele Identifier: CA2278712507

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868693G= , CM000679.2:g.81868693G=	GRCh38
NC_000017.10:g.79826569G= , CM000679.1:g.79826569G=	GRCh37
NC_000017.9:g.77419858G=	NCBI36
NG_034210.1:g.7714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.*183C= MANE Select	ENSP00000269321.7:n.*183C=
ENST00000269321.11:c.*183C=	ENSP00000269321.7:n.*183C=
ENST00000400721.8:c.*183C=	ENSP00000383556.4:n.*183C=
ENST00000541078.6:c.*183C=	ENSP00000441348.2:n.*183C=
ENST00000579121.5:c.503-109C=	ENSP00000462960.1:n.503-109C=
ENST00000580685.5:c.*183C=	ENSP00000464205.1:n.*183C=
ENST00000581876.5:c.*183C=	ENSP00000461956.1:n.*183C=
ENST00000583868.5:c.686C=	ENSP00000462209.1:p.Pro229=
ENST00000584461.5:c.503-109C=	ENSP00000463939.1:n.503-109C=
NM_001185077.2:c.*183C=	NP_001172006.1:n.*183C=
NM_001185078.2:c.*183C=	NP_001172007.1:n.*183C=
NM_001301240.1:c.503-109C=	NP_001288169.1:n.503-109C=
NM_001301241.1:c.503-109C=	NP_001288170.1:n.503-109C=
NM_001301242.1:c.686C=	NP_001288171.1:p.Pro229=
NM_001301243.1:c.*183C=	NP_001288172.1:n.*183C=
NM_004309.5:c.*183C=	NP_004300.1:n.*183C=
NR_125441.1:n.857C=
XM_011523574.1:c.*183C=	XP_011521876.1:n.*183C=
NM_004309.6:c.*183C= MANE Select	NP_004300.1:n.*183C=
NM_001185077.3:c.*183C=	NP_001172006.1:n.*183C=
NM_001185078.3:c.*183C=	NP_001172007.1:n.*183C=
NM_001301240.2:c.503-109C=	NP_001288169.1:n.503-109C=
NM_001301241.2:c.503-109C=	NP_001288170.1:n.503-109C=
NM_001301242.2:c.686C=	NP_001288171.1:p.Pro229=
NM_001301243.2:c.*183C=	NP_001288172.1:n.*183C=
NR_125441.2:n.788C=