Canonical Allele Identifier: CA401523848

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826862T>C (hg19) ; chr17:g.81868986T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868986T>C , CM000679.2:g.81868986T>C	GRCh38
NC_000017.10:g.79826862T>C , CM000679.1:g.79826862T>C	GRCh37
NC_000017.9:g.77420151T>C	NCBI36
NG_034210.1:g.7421A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.505A>G MANE Select	ENSP00000269321.7:p.Met169Val
ENST00000269321.11:c.505A>G	ENSP00000269321.7:p.Met169Val
ENST00000400721.8:c.416-43A>G	ENSP00000383556.4:n.416-43A>G
ENST00000541078.6:c.505A>G	ENSP00000441348.2:p.Met169Val
ENST00000579121.5:c.502+3A>G	ENSP00000462960.1:n.502+3A>G
ENST00000580033.5:c.*149A>G	ENSP00000463530.1:n.*149A>G
ENST00000580685.5:c.505A>G	ENSP00000464205.1:p.Met169Val
ENST00000581876.5:c.280A>G	ENSP00000461956.1:p.Met94Val
ENST00000582984.5:n.707A>G
ENST00000583868.5:c.436-43A>G	ENSP00000462209.1:n.436-43A>G
ENST00000584461.5:c.502+3A>G	ENSP00000463939.1:n.502+3A>G
NM_001185077.2:c.505A>G	NP_001172006.1:p.Met169Val
NM_001185078.2:c.416-43A>G	NP_001172007.1:n.416-43A>G
NM_001301240.1:c.502+3A>G	NP_001288169.1:n.502+3A>G
NM_001301241.1:c.502+3A>G	NP_001288170.1:n.502+3A>G
NM_001301242.1:c.436-43A>G	NP_001288171.1:n.436-43A>G
NM_001301243.1:c.640A>G	NP_001288172.1:p.Met214Val
NM_004309.5:c.505A>G	NP_004300.1:p.Met169Val
NR_125441.1:n.564A>G
XM_011523574.1:c.640A>G	XP_011521876.1:p.Met214Val
NM_004309.6:c.505A>G MANE Select	NP_004300.1:p.Met169Val
NM_001185077.3:c.505A>G	NP_001172006.1:p.Met169Val
NM_001185078.3:c.416-43A>G	NP_001172007.1:n.416-43A>G
NM_001301240.2:c.502+3A>G	NP_001288169.1:n.502+3A>G
NM_001301241.2:c.502+3A>G	NP_001288170.1:n.502+3A>G
NM_001301242.2:c.436-43A>G	NP_001288171.1:n.436-43A>G
NM_001301243.2:c.640A>G	NP_001288172.1:p.Met214Val
NR_125441.2:n.495A>G