Canonical Allele Identifier: CA401522995

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826731C>T (hg19) ; chr17:g.81868855C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868855C>T , CM000679.2:g.81868855C>T	GRCh38
NC_000017.10:g.79826731C>T , CM000679.1:g.79826731C>T	GRCh37
NC_000017.9:g.77420020C>T	NCBI36
NG_034210.1:g.7552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.*21G>A MANE Select	ENSP00000269321.7:n.*21G>A
ENST00000269321.11:c.*21G>A	ENSP00000269321.7:n.*21G>A
ENST00000400721.8:c.*21G>A	ENSP00000383556.4:n.*21G>A
ENST00000541078.6:c.*21G>A	ENSP00000441348.2:n.*21G>A
ENST00000579121.5:c.502+134G>A	ENSP00000462960.1:n.502+134G>A
ENST00000580685.5:c.*21G>A	ENSP00000464205.1:n.*21G>A
ENST00000581876.5:c.*21G>A	ENSP00000461956.1:n.*21G>A
ENST00000583868.5:c.524G>A	ENSP00000462209.1:p.Gly175Glu
ENST00000584461.5:c.502+134G>A	ENSP00000463939.1:n.502+134G>A
NM_001185077.2:c.*21G>A	NP_001172006.1:n.*21G>A
NM_001185078.2:c.*21G>A	NP_001172007.1:n.*21G>A
NM_001301240.1:c.502+134G>A	NP_001288169.1:n.502+134G>A
NM_001301241.1:c.502+134G>A	NP_001288170.1:n.502+134G>A
NM_001301242.1:c.524G>A	NP_001288171.1:p.Gly175Glu
NM_001301243.1:c.*21G>A	NP_001288172.1:n.*21G>A
NM_004309.5:c.*21G>A	NP_004300.1:n.*21G>A
NR_125441.1:n.695G>A
XM_011523574.1:c.*21G>A	XP_011521876.1:n.*21G>A
NM_004309.6:c.*21G>A MANE Select	NP_004300.1:n.*21G>A
NM_001185077.3:c.*21G>A	NP_001172006.1:n.*21G>A
NM_001185078.3:c.*21G>A	NP_001172007.1:n.*21G>A
NM_001301240.2:c.502+134G>A	NP_001288169.1:n.502+134G>A
NM_001301241.2:c.502+134G>A	NP_001288170.1:n.502+134G>A
NM_001301242.2:c.524G>A	NP_001288171.1:p.Gly175Glu
NM_001301243.2:c.*21G>A	NP_001288172.1:n.*21G>A
NR_125441.2:n.626G>A