Canonical Allele Identifier: CA401524589

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79827211A>C (hg19) ; chr17:g.81869335A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869335A>C , CM000679.2:g.81869335A>C	GRCh38
NC_000017.10:g.79827211A>C , CM000679.1:g.79827211A>C	GRCh37
NC_000017.9:g.77420500A>C	NCBI36
NG_034210.1:g.7072T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.346T>G MANE Select	ENSP00000269321.7:p.Phe116Val
ENST00000269321.11:c.346T>G	ENSP00000269321.7:p.Phe116Val
ENST00000400721.8:c.346T>G	ENSP00000383556.4:p.Phe116Val
ENST00000541078.6:c.346T>G	ENSP00000441348.2:p.Phe116Val
ENST00000578351.1:c.275-99T>G	ENSP00000462323.1:n.275-99T>G
ENST00000579121.5:c.346T>G	ENSP00000462960.1:p.Phe116Val
ENST00000580033.5:c.275-99T>G	ENSP00000463530.1:n.275-99T>G
ENST00000580685.5:c.346T>G	ENSP00000464205.1:p.Phe116Val
ENST00000581876.5:c.191-260T>G	ENSP00000461956.1:n.191-260T>G
ENST00000582984.5:n.548T>G
ENST00000583111.5:n.405T>G
ENST00000583791.1:n.117T>G
ENST00000583868.5:c.346T>G	ENSP00000462209.1:p.Phe116Val
ENST00000584397.1:n.589T>G
ENST00000584461.5:c.346T>G	ENSP00000463939.1:p.Phe116Val
NM_001185077.2:c.346T>G	NP_001172006.1:p.Phe116Val
NM_001185078.2:c.346T>G	NP_001172007.1:p.Phe116Val
NM_001301240.1:c.346T>G	NP_001288169.1:p.Phe116Val
NM_001301241.1:c.346T>G	NP_001288170.1:p.Phe116Val
NM_001301242.1:c.346T>G	NP_001288171.1:p.Phe116Val
NM_001301243.1:c.481T>G	NP_001288172.1:p.Phe161Val
NM_004309.5:c.346T>G	NP_004300.1:p.Phe116Val
NR_125441.1:n.411-99T>G
XM_011523574.1:c.481T>G	XP_011521876.1:p.Phe161Val
NM_004309.6:c.346T>G MANE Select	NP_004300.1:p.Phe116Val
NM_001185077.3:c.346T>G	NP_001172006.1:p.Phe116Val
NM_001185078.3:c.346T>G	NP_001172007.1:p.Phe116Val
NM_001301240.2:c.346T>G	NP_001288169.1:p.Phe116Val
NM_001301241.2:c.346T>G	NP_001288170.1:p.Phe116Val
NM_001301242.2:c.346T>G	NP_001288171.1:p.Phe116Val
NM_001301243.2:c.481T>G	NP_001288172.1:p.Phe161Val
NR_125441.2:n.342-99T>G