Canonical Allele Identifier: CA401523301

Gene: ARHGDIA

Linked Data

• dbSNP Id: rs2039163327
• MyVariant Identifiers: chr17:g.79826773G>T (hg19) ; chr17:g.81868897G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868897G>T , CM000679.2:g.81868897G>T	GRCh38
NC_000017.10:g.79826773G>T , CM000679.1:g.79826773G>T	GRCh37
NC_000017.9:g.77420062G>T	NCBI36
NG_034210.1:g.7510C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.594C>A MANE Select	ENSP00000269321.7:p.Ile198=
ENST00000269321.11:c.594C>A	ENSP00000269321.7:p.Ile198=
ENST00000400721.8:c.462C>A	ENSP00000383556.4:p.Ile154=
ENST00000541078.6:c.594C>A	ENSP00000441348.2:p.Ile198=
ENST00000579121.5:c.502+92C>A	ENSP00000462960.1:n.502+92C>A
ENST00000580685.5:c.594C>A	ENSP00000464205.1:p.Ile198=
ENST00000581876.5:c.369C>A	ENSP00000461956.1:p.Ile123=
ENST00000582984.5:n.796C>A
ENST00000583868.5:c.482C>A	ENSP00000462209.1:p.Ser161Ter
ENST00000584461.5:c.502+92C>A	ENSP00000463939.1:n.502+92C>A
NM_001185077.2:c.594C>A	NP_001172006.1:p.Ile198=
NM_001185078.2:c.462C>A	NP_001172007.1:p.Ile154=
NM_001301240.1:c.502+92C>A	NP_001288169.1:n.502+92C>A
NM_001301241.1:c.502+92C>A	NP_001288170.1:n.502+92C>A
NM_001301242.1:c.482C>A	NP_001288171.1:p.Ser161Ter
NM_001301243.1:c.729C>A	NP_001288172.1:p.Ile243=
NM_004309.5:c.594C>A	NP_004300.1:p.Ile198=
NR_125441.1:n.653C>A
XM_011523574.1:c.729C>A	XP_011521876.1:p.Ile243=
NM_004309.6:c.594C>A MANE Select	NP_004300.1:p.Ile198=
NM_001185077.3:c.594C>A	NP_001172006.1:p.Ile198=
NM_001185078.3:c.462C>A	NP_001172007.1:p.Ile154=
NM_001301240.2:c.502+92C>A	NP_001288169.1:n.502+92C>A
NM_001301241.2:c.502+92C>A	NP_001288170.1:n.502+92C>A
NM_001301242.2:c.482C>A	NP_001288171.1:p.Ser161Ter
NM_001301243.2:c.729C>A	NP_001288172.1:p.Ile243=
NR_125441.2:n.584C>A