Canonical Allele Identifier: CA401524004

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826916G>T (hg19) ; chr17:g.81869040G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869040G>T , CM000679.2:g.81869040G>T	GRCh38
NC_000017.10:g.79826916G>T , CM000679.1:g.79826916G>T	GRCh37
NC_000017.9:g.77420205G>T	NCBI36
NG_034210.1:g.7367C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.451C>A MANE Select	ENSP00000269321.7:p.Pro151Thr
ENST00000269321.11:c.451C>A	ENSP00000269321.7:p.Pro151Thr
ENST00000400721.8:c.416-97C>A	ENSP00000383556.4:n.416-97C>A
ENST00000541078.6:c.451C>A	ENSP00000441348.2:p.Pro151Thr
ENST00000579121.5:c.451C>A	ENSP00000462960.1:p.Pro151Thr
ENST00000580033.5:c.*95C>A	ENSP00000463530.1:n.*95C>A
ENST00000580685.5:c.451C>A	ENSP00000464205.1:p.Pro151Thr
ENST00000581876.5:c.226C>A	ENSP00000461956.1:p.Pro76Thr
ENST00000582984.5:n.653C>A
ENST00000583791.1:n.315C>A
ENST00000583868.5:c.435+16C>A	ENSP00000462209.1:n.435+16C>A
ENST00000584461.5:c.451C>A	ENSP00000463939.1:p.Pro151Thr
NM_001185077.2:c.451C>A	NP_001172006.1:p.Pro151Thr
NM_001185078.2:c.416-97C>A	NP_001172007.1:n.416-97C>A
NM_001301240.1:c.451C>A	NP_001288169.1:p.Pro151Thr
NM_001301241.1:c.451C>A	NP_001288170.1:p.Pro151Thr
NM_001301242.1:c.435+16C>A	NP_001288171.1:n.435+16C>A
NM_001301243.1:c.586C>A	NP_001288172.1:p.Pro196Thr
NM_004309.5:c.451C>A	NP_004300.1:p.Pro151Thr
NR_125441.1:n.510C>A
XM_011523574.1:c.586C>A	XP_011521876.1:p.Pro196Thr
NM_004309.6:c.451C>A MANE Select	NP_004300.1:p.Pro151Thr
NM_001185077.3:c.451C>A	NP_001172006.1:p.Pro151Thr
NM_001185078.3:c.416-97C>A	NP_001172007.1:n.416-97C>A
NM_001301240.2:c.451C>A	NP_001288169.1:p.Pro151Thr
NM_001301241.2:c.451C>A	NP_001288170.1:p.Pro151Thr
NM_001301242.2:c.435+16C>A	NP_001288171.1:n.435+16C>A
NM_001301243.2:c.586C>A	NP_001288172.1:p.Pro196Thr
NR_125441.2:n.441C>A