Canonical Allele Identifier: CA401523830

Gene: ARHGDIA

Linked Data

• gnomAD v4: 17-81868983-G-C
• MyVariant Identifiers: chr17:g.79826859G>C (hg19) ; chr17:g.81868983G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868983G>C , CM000679.2:g.81868983G>C	GRCh38
NC_000017.10:g.79826859G>C , CM000679.1:g.79826859G>C	GRCh37
NC_000017.9:g.77420148G>C	NCBI36
NG_034210.1:g.7424C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.508C>G MANE Select	ENSP00000269321.7:p.Leu170Val
ENST00000269321.11:c.508C>G	ENSP00000269321.7:p.Leu170Val
ENST00000400721.8:c.416-40C>G	ENSP00000383556.4:n.416-40C>G
ENST00000541078.6:c.508C>G	ENSP00000441348.2:p.Leu170Val
ENST00000579121.5:c.502+6C>G	ENSP00000462960.1:n.502+6C>G
ENST00000580033.5:c.*152C>G	ENSP00000463530.1:n.*152C>G
ENST00000580685.5:c.508C>G	ENSP00000464205.1:p.Leu170Val
ENST00000581876.5:c.283C>G	ENSP00000461956.1:p.Leu95Val
ENST00000582984.5:n.710C>G
ENST00000583868.5:c.436-40C>G	ENSP00000462209.1:n.436-40C>G
ENST00000584461.5:c.502+6C>G	ENSP00000463939.1:n.502+6C>G
NM_001185077.2:c.508C>G	NP_001172006.1:p.Leu170Val
NM_001185078.2:c.416-40C>G	NP_001172007.1:n.416-40C>G
NM_001301240.1:c.502+6C>G	NP_001288169.1:n.502+6C>G
NM_001301241.1:c.502+6C>G	NP_001288170.1:n.502+6C>G
NM_001301242.1:c.436-40C>G	NP_001288171.1:n.436-40C>G
NM_001301243.1:c.643C>G	NP_001288172.1:p.Leu215Val
NM_004309.5:c.508C>G	NP_004300.1:p.Leu170Val
NR_125441.1:n.567C>G
XM_011523574.1:c.643C>G	XP_011521876.1:p.Leu215Val
NM_004309.6:c.508C>G MANE Select	NP_004300.1:p.Leu170Val
NM_001185077.3:c.508C>G	NP_001172006.1:p.Leu170Val
NM_001185078.3:c.416-40C>G	NP_001172007.1:n.416-40C>G
NM_001301240.2:c.502+6C>G	NP_001288169.1:n.502+6C>G
NM_001301241.2:c.502+6C>G	NP_001288170.1:n.502+6C>G
NM_001301242.2:c.436-40C>G	NP_001288171.1:n.436-40C>G
NM_001301243.2:c.643C>G	NP_001288172.1:p.Leu215Val
NR_125441.2:n.498C>G