Canonical Allele Identifier: CA401523212

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826761C>A (hg19) ; chr17:g.81868885C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868885C>A , CM000679.2:g.81868885C>A	GRCh38
NC_000017.10:g.79826761C>A , CM000679.1:g.79826761C>A	GRCh37
NC_000017.9:g.77420050C>A	NCBI36
NG_034210.1:g.7522G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.606G>T MANE Select	ENSP00000269321.7:p.Trp202Cys
ENST00000269321.11:c.606G>T	ENSP00000269321.7:p.Trp202Cys
ENST00000400721.8:c.474G>T	ENSP00000383556.4:p.Trp158Cys
ENST00000541078.6:c.606G>T	ENSP00000441348.2:p.Trp202Cys
ENST00000579121.5:c.502+104G>T	ENSP00000462960.1:n.502+104G>T
ENST00000580685.5:c.606G>T	ENSP00000464205.1:p.Trp202Cys
ENST00000581876.5:c.381G>T	ENSP00000461956.1:p.Trp127Cys
ENST00000582984.5:n.808G>T
ENST00000583868.5:c.494G>T	ENSP00000462209.1:p.Gly165Val
ENST00000584461.5:c.502+104G>T	ENSP00000463939.1:n.502+104G>T
NM_001185077.2:c.606G>T	NP_001172006.1:p.Trp202Cys
NM_001185078.2:c.474G>T	NP_001172007.1:p.Trp158Cys
NM_001301240.1:c.502+104G>T	NP_001288169.1:n.502+104G>T
NM_001301241.1:c.502+104G>T	NP_001288170.1:n.502+104G>T
NM_001301242.1:c.494G>T	NP_001288171.1:p.Gly165Val
NM_001301243.1:c.741G>T	NP_001288172.1:p.Trp247Cys
NM_004309.5:c.606G>T	NP_004300.1:p.Trp202Cys
NR_125441.1:n.665G>T
XM_011523574.1:c.741G>T	XP_011521876.1:p.Trp247Cys
NM_004309.6:c.606G>T MANE Select	NP_004300.1:p.Trp202Cys
NM_001185077.3:c.606G>T	NP_001172006.1:p.Trp202Cys
NM_001185078.3:c.474G>T	NP_001172007.1:p.Trp158Cys
NM_001301240.2:c.502+104G>T	NP_001288169.1:n.502+104G>T
NM_001301241.2:c.502+104G>T	NP_001288170.1:n.502+104G>T
NM_001301242.2:c.494G>T	NP_001288171.1:p.Gly165Val
NM_001301243.2:c.741G>T	NP_001288172.1:p.Trp247Cys
NR_125441.2:n.596G>T