Canonical Allele Identifier: CA401523331

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826776G>C (hg19) ; chr17:g.81868900G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868900G>C , CM000679.2:g.81868900G>C	GRCh38
NC_000017.10:g.79826776G>C , CM000679.1:g.79826776G>C	GRCh37
NC_000017.9:g.77420065G>C	NCBI36
NG_034210.1:g.7507C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.591C>G MANE Select	ENSP00000269321.7:p.Thr197=
ENST00000269321.11:c.591C>G	ENSP00000269321.7:p.Thr197=
ENST00000400721.8:c.459C>G	ENSP00000383556.4:p.Thr153=
ENST00000541078.6:c.591C>G	ENSP00000441348.2:p.Thr197=
ENST00000579121.5:c.502+89C>G	ENSP00000462960.1:n.502+89C>G
ENST00000580685.5:c.591C>G	ENSP00000464205.1:p.Thr197=
ENST00000581876.5:c.366C>G	ENSP00000461956.1:p.Thr122=
ENST00000582984.5:n.793C>G
ENST00000583868.5:c.479C>G	ENSP00000462209.1:p.Pro160Arg
ENST00000584461.5:c.502+89C>G	ENSP00000463939.1:n.502+89C>G
NM_001185077.2:c.591C>G	NP_001172006.1:p.Thr197=
NM_001185078.2:c.459C>G	NP_001172007.1:p.Thr153=
NM_001301240.1:c.502+89C>G	NP_001288169.1:n.502+89C>G
NM_001301241.1:c.502+89C>G	NP_001288170.1:n.502+89C>G
NM_001301242.1:c.479C>G	NP_001288171.1:p.Pro160Arg
NM_001301243.1:c.726C>G	NP_001288172.1:p.Thr242=
NM_004309.5:c.591C>G	NP_004300.1:p.Thr197=
NR_125441.1:n.650C>G
XM_011523574.1:c.726C>G	XP_011521876.1:p.Thr242=
NM_004309.6:c.591C>G MANE Select	NP_004300.1:p.Thr197=
NM_001185077.3:c.591C>G	NP_001172006.1:p.Thr197=
NM_001185078.3:c.459C>G	NP_001172007.1:p.Thr153=
NM_001301240.2:c.502+89C>G	NP_001288169.1:n.502+89C>G
NM_001301241.2:c.502+89C>G	NP_001288170.1:n.502+89C>G
NM_001301242.2:c.479C>G	NP_001288171.1:p.Pro160Arg
NM_001301243.2:c.726C>G	NP_001288172.1:p.Thr242=
NR_125441.2:n.581C>G