Canonical Allele Identifier: CA2278712681

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868906A= , CM000679.2:g.81868906A=	GRCh38
NC_000017.10:g.79826782A= , CM000679.1:g.79826782A=	GRCh37
NC_000017.9:g.77420071A=	NCBI36
NG_034210.1:g.7501T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.585T= MANE Select	ENSP00000269321.7:p.Asn195=
ENST00000269321.11:c.585T=	ENSP00000269321.7:p.Asn195=
ENST00000400721.8:c.453T=	ENSP00000383556.4:p.Asn151=
ENST00000541078.6:c.585T=	ENSP00000441348.2:p.Asn195=
ENST00000579121.5:c.502+83T=	ENSP00000462960.1:n.502+83T=
ENST00000580685.5:c.585T=	ENSP00000464205.1:p.Asn195=
ENST00000581876.5:c.360T=	ENSP00000461956.1:p.Asn120=
ENST00000582984.5:n.787T=
ENST00000583868.5:c.473T=	ENSP00000462209.1:p.Ile158=
ENST00000584461.5:c.502+83T=	ENSP00000463939.1:n.502+83T=
NM_001185077.2:c.585T=	NP_001172006.1:p.Asn195=
NM_001185078.2:c.453T=	NP_001172007.1:p.Asn151=
NM_001301240.1:c.502+83T=	NP_001288169.1:n.502+83T=
NM_001301241.1:c.502+83T=	NP_001288170.1:n.502+83T=
NM_001301242.1:c.473T=	NP_001288171.1:p.Ile158=
NM_001301243.1:c.720T=	NP_001288172.1:p.Asn240=
NM_004309.5:c.585T=	NP_004300.1:p.Asn195=
NR_125441.1:n.644T=
XM_011523574.1:c.720T=	XP_011521876.1:p.Asn240=
NM_004309.6:c.585T= MANE Select	NP_004300.1:p.Asn195=
NM_001185077.3:c.585T=	NP_001172006.1:p.Asn195=
NM_001185078.3:c.453T=	NP_001172007.1:p.Asn151=
NM_001301240.2:c.502+83T=	NP_001288169.1:n.502+83T=
NM_001301241.2:c.502+83T=	NP_001288170.1:n.502+83T=
NM_001301242.2:c.473T=	NP_001288171.1:p.Ile158=
NM_001301243.2:c.720T=	NP_001288172.1:p.Asn240=
NR_125441.2:n.575T=