Canonical Allele Identifier: CA401522974

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826726T>C (hg19) ; chr17:g.81868850T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868850T>C , CM000679.2:g.81868850T>C	GRCh38
NC_000017.10:g.79826726T>C , CM000679.1:g.79826726T>C	GRCh37
NC_000017.9:g.77420015T>C	NCBI36
NG_034210.1:g.7557A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.*26A>G MANE Select	ENSP00000269321.7:n.*26A>G
ENST00000269321.11:c.*26A>G	ENSP00000269321.7:n.*26A>G
ENST00000400721.8:c.*26A>G	ENSP00000383556.4:n.*26A>G
ENST00000541078.6:c.*26A>G	ENSP00000441348.2:n.*26A>G
ENST00000579121.5:c.502+139A>G	ENSP00000462960.1:n.502+139A>G
ENST00000580685.5:c.*26A>G	ENSP00000464205.1:n.*26A>G
ENST00000581876.5:c.*26A>G	ENSP00000461956.1:n.*26A>G
ENST00000583868.5:c.529A>G	ENSP00000462209.1:p.Thr177Ala
ENST00000584461.5:c.502+139A>G	ENSP00000463939.1:n.502+139A>G
NM_001185077.2:c.*26A>G	NP_001172006.1:n.*26A>G
NM_001185078.2:c.*26A>G	NP_001172007.1:n.*26A>G
NM_001301240.1:c.502+139A>G	NP_001288169.1:n.502+139A>G
NM_001301241.1:c.502+139A>G	NP_001288170.1:n.502+139A>G
NM_001301242.1:c.529A>G	NP_001288171.1:p.Thr177Ala
NM_001301243.1:c.*26A>G	NP_001288172.1:n.*26A>G
NM_004309.5:c.*26A>G	NP_004300.1:n.*26A>G
NR_125441.1:n.700A>G
XM_011523574.1:c.*26A>G	XP_011521876.1:n.*26A>G
NM_004309.6:c.*26A>G MANE Select	NP_004300.1:n.*26A>G
NM_001185077.3:c.*26A>G	NP_001172006.1:n.*26A>G
NM_001185078.3:c.*26A>G	NP_001172007.1:n.*26A>G
NM_001301240.2:c.502+139A>G	NP_001288169.1:n.502+139A>G
NM_001301241.2:c.502+139A>G	NP_001288170.1:n.502+139A>G
NM_001301242.2:c.529A>G	NP_001288171.1:p.Thr177Ala
NM_001301243.2:c.*26A>G	NP_001288172.1:n.*26A>G
NR_125441.2:n.631A>G