Canonical Allele Identifier: CA2581331673

Gene: ARHGDIA

Linked Data

• gnomAD v4: 17-81869287-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869287C>G , CM000679.2:g.81869287C>G	GRCh38
NC_000017.10:g.79827163C>G , CM000679.1:g.79827163C>G	GRCh37
NC_000017.9:g.77420452C>G	NCBI36
NG_034210.1:g.7120G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.351+43G>C MANE Select	ENSP00000269321.7:n.351+43G>C
ENST00000269321.11:c.351+43G>C	ENSP00000269321.7:n.351+43G>C
ENST00000400721.8:c.351+43G>C	ENSP00000383556.4:n.351+43G>C
ENST00000541078.6:c.351+43G>C	ENSP00000441348.2:n.351+43G>C
ENST00000578351.1:c.275-51G>C	ENSP00000462323.1:n.275-51G>C
ENST00000579121.5:c.351+43G>C	ENSP00000462960.1:n.351+43G>C
ENST00000580033.5:c.275-51G>C	ENSP00000463530.1:n.275-51G>C
ENST00000580685.5:c.351+43G>C	ENSP00000464205.1:n.351+43G>C
ENST00000581876.5:c.191-212G>C	ENSP00000461956.1:n.191-212G>C
ENST00000582984.5:n.553+43G>C
ENST00000583111.5:n.453G>C
ENST00000583791.1:n.165G>C
ENST00000583868.5:c.351+43G>C	ENSP00000462209.1:n.351+43G>C
ENST00000584461.5:c.351+43G>C	ENSP00000463939.1:n.351+43G>C
NM_001185077.2:c.351+43G>C	NP_001172006.1:n.351+43G>C
NM_001185078.2:c.351+43G>C	NP_001172007.1:n.351+43G>C
NM_001301240.1:c.351+43G>C	NP_001288169.1:n.351+43G>C
NM_001301241.1:c.351+43G>C	NP_001288170.1:n.351+43G>C
NM_001301242.1:c.351+43G>C	NP_001288171.1:n.351+43G>C
NM_001301243.1:c.486+43G>C	NP_001288172.1:n.486+43G>C
NM_004309.5:c.351+43G>C	NP_004300.1:n.351+43G>C
NR_125441.1:n.411-51G>C
XM_011523574.1:c.486+43G>C	XP_011521876.1:n.486+43G>C
NM_004309.6:c.351+43G>C MANE Select	NP_004300.1:n.351+43G>C
NM_001185077.3:c.351+43G>C	NP_001172006.1:n.351+43G>C
NM_001185078.3:c.351+43G>C	NP_001172007.1:n.351+43G>C
NM_001301240.2:c.351+43G>C	NP_001288169.1:n.351+43G>C
NM_001301241.2:c.351+43G>C	NP_001288170.1:n.351+43G>C
NM_001301242.2:c.351+43G>C	NP_001288171.1:n.351+43G>C
NM_001301243.2:c.486+43G>C	NP_001288172.1:n.486+43G>C
NR_125441.2:n.342-51G>C