Canonical Allele Identifier: CA2278712743

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869039G= , CM000679.2:g.81869039G=	GRCh38
NC_000017.10:g.79826915G= , CM000679.1:g.79826915G=	GRCh37
NC_000017.9:g.77420204G=	NCBI36
NG_034210.1:g.7368C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.452C= MANE Select	ENSP00000269321.7:p.Pro151=
ENST00000269321.11:c.452C=	ENSP00000269321.7:p.Pro151=
ENST00000400721.8:c.416-96C=	ENSP00000383556.4:n.416-96C=
ENST00000541078.6:c.452C=	ENSP00000441348.2:p.Pro151=
ENST00000579121.5:c.452C=	ENSP00000462960.1:p.Pro151=
ENST00000580033.5:c.*96C=	ENSP00000463530.1:n.*96C=
ENST00000580685.5:c.452C=	ENSP00000464205.1:p.Pro151=
ENST00000581876.5:c.227C=	ENSP00000461956.1:p.Pro76=
ENST00000582984.5:n.654C=
ENST00000583791.1:n.316C=
ENST00000583868.5:c.435+17C=	ENSP00000462209.1:n.435+17C=
ENST00000584461.5:c.452C=	ENSP00000463939.1:p.Pro151=
NM_001185077.2:c.452C=	NP_001172006.1:p.Pro151=
NM_001185078.2:c.416-96C=	NP_001172007.1:n.416-96C=
NM_001301240.1:c.452C=	NP_001288169.1:p.Pro151=
NM_001301241.1:c.452C=	NP_001288170.1:p.Pro151=
NM_001301242.1:c.435+17C=	NP_001288171.1:n.435+17C=
NM_001301243.1:c.587C=	NP_001288172.1:p.Pro196=
NM_004309.5:c.452C=	NP_004300.1:p.Pro151=
NR_125441.1:n.511C=
XM_011523574.1:c.587C=	XP_011521876.1:p.Pro196=
NM_004309.6:c.452C= MANE Select	NP_004300.1:p.Pro151=
NM_001185077.3:c.452C=	NP_001172006.1:p.Pro151=
NM_001185078.3:c.416-96C=	NP_001172007.1:n.416-96C=
NM_001301240.2:c.452C=	NP_001288169.1:p.Pro151=
NM_001301241.2:c.452C=	NP_001288170.1:p.Pro151=
NM_001301242.2:c.435+17C=	NP_001288171.1:n.435+17C=
NM_001301243.2:c.587C=	NP_001288172.1:p.Pro196=
NR_125441.2:n.442C=