Canonical Allele Identifier: CA2278712711

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868980C= , CM000679.2:g.81868980C=	GRCh38
NC_000017.10:g.79826856C= , CM000679.1:g.79826856C=	GRCh37
NC_000017.9:g.77420145C=	NCBI36
NG_034210.1:g.7427G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.511G= MANE Select	ENSP00000269321.7:p.Ala171=
ENST00000269321.11:c.511G=	ENSP00000269321.7:p.Ala171=
ENST00000400721.8:c.416-37G=	ENSP00000383556.4:n.416-37G=
ENST00000541078.6:c.511G=	ENSP00000441348.2:p.Ala171=
ENST00000579121.5:c.502+9G=	ENSP00000462960.1:n.502+9G=
ENST00000580033.5:c.*155G=	ENSP00000463530.1:n.*155G=
ENST00000580685.5:c.511G=	ENSP00000464205.1:p.Ala171=
ENST00000581876.5:c.286G=	ENSP00000461956.1:p.Ala96=
ENST00000582984.5:n.713G=
ENST00000583868.5:c.436-37G=	ENSP00000462209.1:n.436-37G=
ENST00000584461.5:c.502+9G=	ENSP00000463939.1:n.502+9G=
NM_001185077.2:c.511G=	NP_001172006.1:p.Ala171=
NM_001185078.2:c.416-37G=	NP_001172007.1:n.416-37G=
NM_001301240.1:c.502+9G=	NP_001288169.1:n.502+9G=
NM_001301241.1:c.502+9G=	NP_001288170.1:n.502+9G=
NM_001301242.1:c.436-37G=	NP_001288171.1:n.436-37G=
NM_001301243.1:c.646G=	NP_001288172.1:p.Ala216=
NM_004309.5:c.511G=	NP_004300.1:p.Ala171=
NR_125441.1:n.570G=
XM_011523574.1:c.646G=	XP_011521876.1:p.Ala216=
NM_004309.6:c.511G= MANE Select	NP_004300.1:p.Ala171=
NM_001185077.3:c.511G=	NP_001172006.1:p.Ala171=
NM_001185078.3:c.416-37G=	NP_001172007.1:n.416-37G=
NM_001301240.2:c.502+9G=	NP_001288169.1:n.502+9G=
NM_001301241.2:c.502+9G=	NP_001288170.1:n.502+9G=
NM_001301242.2:c.436-37G=	NP_001288171.1:n.436-37G=
NM_001301243.2:c.646G=	NP_001288172.1:p.Ala216=
NR_125441.2:n.501G=