Canonical Allele Identifier: CA401523856

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826864C>A (hg19) ; chr17:g.81868988C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868988C>A , CM000679.2:g.81868988C>A	GRCh38
NC_000017.10:g.79826864C>A , CM000679.1:g.79826864C>A	GRCh37
NC_000017.9:g.77420153C>A	NCBI36
NG_034210.1:g.7419G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.503G>T MANE Select	ENSP00000269321.7:p.Gly168Val
ENST00000269321.11:c.503G>T	ENSP00000269321.7:p.Gly168Val
ENST00000400721.8:c.416-45G>T	ENSP00000383556.4:n.416-45G>T
ENST00000541078.6:c.503G>T	ENSP00000441348.2:p.Gly168Val
ENST00000579121.5:c.502+1G>T	ENSP00000462960.1:n.502+1G>T
ENST00000580033.5:c.*147G>T	ENSP00000463530.1:n.*147G>T
ENST00000580685.5:c.503G>T	ENSP00000464205.1:p.Gly168Val
ENST00000581876.5:c.278G>T	ENSP00000461956.1:p.Gly93Val
ENST00000582984.5:n.705G>T
ENST00000583868.5:c.436-45G>T	ENSP00000462209.1:n.436-45G>T
ENST00000584461.5:c.502+1G>T	ENSP00000463939.1:n.502+1G>T
NM_001185077.2:c.503G>T	NP_001172006.1:p.Gly168Val
NM_001185078.2:c.416-45G>T	NP_001172007.1:n.416-45G>T
NM_001301240.1:c.502+1G>T	NP_001288169.1:n.502+1G>T
NM_001301241.1:c.502+1G>T	NP_001288170.1:n.502+1G>T
NM_001301242.1:c.436-45G>T	NP_001288171.1:n.436-45G>T
NM_001301243.1:c.638G>T	NP_001288172.1:p.Gly213Val
NM_004309.5:c.503G>T	NP_004300.1:p.Gly168Val
NR_125441.1:n.562G>T
XM_011523574.1:c.638G>T	XP_011521876.1:p.Gly213Val
NM_004309.6:c.503G>T MANE Select	NP_004300.1:p.Gly168Val
NM_001185077.3:c.503G>T	NP_001172006.1:p.Gly168Val
NM_001185078.3:c.416-45G>T	NP_001172007.1:n.416-45G>T
NM_001301240.2:c.502+1G>T	NP_001288169.1:n.502+1G>T
NM_001301241.2:c.502+1G>T	NP_001288170.1:n.502+1G>T
NM_001301242.2:c.436-45G>T	NP_001288171.1:n.436-45G>T
NM_001301243.2:c.638G>T	NP_001288172.1:p.Gly213Val
NR_125441.2:n.493G>T