Canonical Allele Identifier: CA401524455

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79827098T>C (hg19) ; chr17:g.81869222T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869222T>C , CM000679.2:g.81869222T>C	GRCh38
NC_000017.10:g.79827098T>C , CM000679.1:g.79827098T>C	GRCh37
NC_000017.9:g.77420387T>C	NCBI36
NG_034210.1:g.7185A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.366A>G MANE Select	ENSP00000269321.7:p.Ile122Met
ENST00000269321.11:c.366A>G	ENSP00000269321.7:p.Ile122Met
ENST00000400721.8:c.366A>G	ENSP00000383556.4:p.Ile122Met
ENST00000541078.6:c.366A>G	ENSP00000441348.2:p.Ile122Met
ENST00000578351.1:c.*10A>G	ENSP00000462323.1:n.*10A>G
ENST00000579121.5:c.366A>G	ENSP00000462960.1:p.Ile122Met
ENST00000580033.5:c.*10A>G	ENSP00000463530.1:n.*10A>G
ENST00000580685.5:c.366A>G	ENSP00000464205.1:p.Ile122Met
ENST00000581876.5:c.191-147A>G	ENSP00000461956.1:n.191-147A>G
ENST00000582984.5:n.568A>G
ENST00000583111.5:n.518A>G
ENST00000583791.1:n.230A>G
ENST00000583868.5:c.366A>G	ENSP00000462209.1:p.Ile122Met
ENST00000584461.5:c.366A>G	ENSP00000463939.1:p.Ile122Met
NM_001185077.2:c.366A>G	NP_001172006.1:p.Ile122Met
NM_001185078.2:c.366A>G	NP_001172007.1:p.Ile122Met
NM_001301240.1:c.366A>G	NP_001288169.1:p.Ile122Met
NM_001301241.1:c.366A>G	NP_001288170.1:p.Ile122Met
NM_001301242.1:c.366A>G	NP_001288171.1:p.Ile122Met
NM_001301243.1:c.501A>G	NP_001288172.1:p.Ile167Met
NM_004309.5:c.366A>G	NP_004300.1:p.Ile122Met
NR_125441.1:n.425A>G
XM_011523574.1:c.501A>G	XP_011521876.1:p.Ile167Met
NM_004309.6:c.366A>G MANE Select	NP_004300.1:p.Ile122Met
NM_001185077.3:c.366A>G	NP_001172006.1:p.Ile122Met
NM_001185078.3:c.366A>G	NP_001172007.1:p.Ile122Met
NM_001301240.2:c.366A>G	NP_001288169.1:p.Ile122Met
NM_001301241.2:c.366A>G	NP_001288170.1:p.Ile122Met
NM_001301242.2:c.366A>G	NP_001288171.1:p.Ile122Met
NM_001301243.2:c.501A>G	NP_001288172.1:p.Ile167Met
NR_125441.2:n.356A>G