Canonical Allele Identifier: CA775682779
Gene: ARHGDIA HGNC NCBI

Linked Data

dbSNP Id: rs955615883

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81869259C>A , CM000679.2:g.81869259C>A GRCh38
NC_000017.10:g.79827135C>A , CM000679.1:g.79827135C>A GRCh37
NC_000017.9:g.77420424C>A NCBI36
NG_034210.1:g.7148G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000269321.12:c.352-23G>T MANE Select ENSP00000269321.7:n.352-23G>T
ENST00000269321.11:c.352-23G>T ENSP00000269321.7:n.352-23G>T
ENST00000400721.8:c.352-23G>T ENSP00000383556.4:n.352-23G>T
ENST00000541078.6:c.352-23G>T ENSP00000441348.2:n.352-23G>T
ENST00000578351.1:c.275-23G>T ENSP00000462323.1:n.275-23G>T
ENST00000579121.5:c.352-23G>T ENSP00000462960.1:n.352-23G>T
ENST00000580033.5:c.275-23G>T ENSP00000463530.1:n.275-23G>T
ENST00000580685.5:c.352-23G>T ENSP00000464205.1:n.352-23G>T
ENST00000581876.5:c.191-184G>T ENSP00000461956.1:n.191-184G>T
ENST00000582984.5:n.554-23G>T
ENST00000583111.5:n.481G>T
ENST00000583791.1:n.193G>T
ENST00000583868.5:c.352-23G>T ENSP00000462209.1:n.352-23G>T
ENST00000584461.5:c.352-23G>T ENSP00000463939.1:n.352-23G>T
NM_001185077.2:c.352-23G>T NP_001172006.1:n.352-23G>T
NM_001185078.2:c.352-23G>T NP_001172007.1:n.352-23G>T
NM_001301240.1:c.352-23G>T NP_001288169.1:n.352-23G>T
NM_001301241.1:c.352-23G>T NP_001288170.1:n.352-23G>T
NM_001301242.1:c.352-23G>T NP_001288171.1:n.352-23G>T
NM_001301243.1:c.487-23G>T NP_001288172.1:n.487-23G>T
NM_004309.5:c.352-23G>T NP_004300.1:n.352-23G>T
NR_125441.1:n.411-23G>T
XM_011523574.1:c.487-23G>T XP_011521876.1:n.487-23G>T
NM_004309.6:c.352-23G>T MANE Select NP_004300.1:n.352-23G>T
NM_001185077.3:c.352-23G>T NP_001172006.1:n.352-23G>T
NM_001185078.3:c.352-23G>T NP_001172007.1:n.352-23G>T
NM_001301240.2:c.352-23G>T NP_001288169.1:n.352-23G>T
NM_001301241.2:c.352-23G>T NP_001288170.1:n.352-23G>T
NM_001301242.2:c.352-23G>T NP_001288171.1:n.352-23G>T
NM_001301243.2:c.487-23G>T NP_001288172.1:n.487-23G>T
NR_125441.2:n.342-23G>T