Canonical Allele Identifier: CA2278712683

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868912C= , CM000679.2:g.81868912C=	GRCh38
NC_000017.10:g.79826788C= , CM000679.1:g.79826788C=	GRCh37
NC_000017.9:g.77420077C=	NCBI36
NG_034210.1:g.7495G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.579G= MANE Select	ENSP00000269321.7:p.Glu193=
ENST00000269321.11:c.579G=	ENSP00000269321.7:p.Glu193=
ENST00000400721.8:c.447G=	ENSP00000383556.4:p.Glu149=
ENST00000541078.6:c.579G=	ENSP00000441348.2:p.Glu193=
ENST00000579121.5:c.502+77G=	ENSP00000462960.1:n.502+77G=
ENST00000580685.5:c.579G=	ENSP00000464205.1:p.Glu193=
ENST00000581876.5:c.354G=	ENSP00000461956.1:p.Glu118=
ENST00000582984.5:n.781G=
ENST00000583868.5:c.467G=	ENSP00000462209.1:p.Ser156=
ENST00000584461.5:c.502+77G=	ENSP00000463939.1:n.502+77G=
NM_001185077.2:c.579G=	NP_001172006.1:p.Glu193=
NM_001185078.2:c.447G=	NP_001172007.1:p.Glu149=
NM_001301240.1:c.502+77G=	NP_001288169.1:n.502+77G=
NM_001301241.1:c.502+77G=	NP_001288170.1:n.502+77G=
NM_001301242.1:c.467G=	NP_001288171.1:p.Ser156=
NM_001301243.1:c.714G=	NP_001288172.1:p.Glu238=
NM_004309.5:c.579G=	NP_004300.1:p.Glu193=
NR_125441.1:n.638G=
XM_011523574.1:c.714G=	XP_011521876.1:p.Glu238=
NM_004309.6:c.579G= MANE Select	NP_004300.1:p.Glu193=
NM_001185077.3:c.579G=	NP_001172006.1:p.Glu193=
NM_001185078.3:c.447G=	NP_001172007.1:p.Glu149=
NM_001301240.2:c.502+77G=	NP_001288169.1:n.502+77G=
NM_001301241.2:c.502+77G=	NP_001288170.1:n.502+77G=
NM_001301242.2:c.467G=	NP_001288171.1:p.Ser156=
NM_001301243.2:c.714G=	NP_001288172.1:p.Glu238=
NR_125441.2:n.569G=