Canonical Allele Identifier: CA401523502

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826800G>C (hg19) ; chr17:g.81868924G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868924G>C , CM000679.2:g.81868924G>C	GRCh38
NC_000017.10:g.79826800G>C , CM000679.1:g.79826800G>C	GRCh37
NC_000017.9:g.77420089G>C	NCBI36
NG_034210.1:g.7483C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.567C>G MANE Select	ENSP00000269321.7:p.His189Gln
ENST00000269321.11:c.567C>G	ENSP00000269321.7:p.His189Gln
ENST00000400721.8:c.435C>G	ENSP00000383556.4:p.His145Gln
ENST00000541078.6:c.567C>G	ENSP00000441348.2:p.His189Gln
ENST00000579121.5:c.502+65C>G	ENSP00000462960.1:n.502+65C>G
ENST00000580033.5:c.*211C>G	ENSP00000463530.1:n.*211C>G
ENST00000580685.5:c.567C>G	ENSP00000464205.1:p.His189Gln
ENST00000581876.5:c.342C>G	ENSP00000461956.1:p.His114Gln
ENST00000582984.5:n.769C>G
ENST00000583868.5:c.455C>G	ENSP00000462209.1:p.Thr152Ser
ENST00000584461.5:c.502+65C>G	ENSP00000463939.1:n.502+65C>G
NM_001185077.2:c.567C>G	NP_001172006.1:p.His189Gln
NM_001185078.2:c.435C>G	NP_001172007.1:p.His145Gln
NM_001301240.1:c.502+65C>G	NP_001288169.1:n.502+65C>G
NM_001301241.1:c.502+65C>G	NP_001288170.1:n.502+65C>G
NM_001301242.1:c.455C>G	NP_001288171.1:p.Thr152Ser
NM_001301243.1:c.702C>G	NP_001288172.1:p.His234Gln
NM_004309.5:c.567C>G	NP_004300.1:p.His189Gln
NR_125441.1:n.626C>G
XM_011523574.1:c.702C>G	XP_011521876.1:p.His234Gln
NM_004309.6:c.567C>G MANE Select	NP_004300.1:p.His189Gln
NM_001185077.3:c.567C>G	NP_001172006.1:p.His189Gln
NM_001185078.3:c.435C>G	NP_001172007.1:p.His145Gln
NM_001301240.2:c.502+65C>G	NP_001288169.1:n.502+65C>G
NM_001301241.2:c.502+65C>G	NP_001288170.1:n.502+65C>G
NM_001301242.2:c.455C>G	NP_001288171.1:p.Thr152Ser
NM_001301243.2:c.702C>G	NP_001288172.1:p.His234Gln
NR_125441.2:n.557C>G