Canonical Allele Identifier: CA628024154
Gene: ARHGDIA HGNC NCBI

Linked Data

dbSNP Id: rs779870102

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868840_81868847del , CM000679.2:g.81868840_81868847del GRCh38
NC_000017.10:g.79826716_79826723del , CM000679.1:g.79826716_79826723del GRCh37
NC_000017.9:g.77420005_77420012del NCBI36
NG_034210.1:g.7564_7571del

Transcript Alleles

HGVS Amino-acid change
ENST00000269321.12:c.*33_*40del MANE Select ENSP00000269321.7:n.*33_*40del
ENST00000269321.11:c.*33_*40del ENSP00000269321.7:n.*33_*40del
ENST00000400721.8:c.*33_*40del ENSP00000383556.4:n.*33_*40del
ENST00000541078.6:c.*33_*40del ENSP00000441348.2:n.*33_*40del
ENST00000579121.5:c.502+146_502+153del ENSP00000462960.1:n.502+146_502+153del
ENST00000580685.5:c.*33_*40del ENSP00000464205.1:n.*33_*40del
ENST00000581876.5:c.*33_*40del ENSP00000461956.1:n.*33_*40del
ENST00000583868.5:c.536_543del ENSP00000462209.1:p.Gly179AspfsTer19
ENST00000584461.5:c.502+146_502+153del ENSP00000463939.1:n.502+146_502+153del
NM_001185077.2:c.*33_*40del NP_001172006.1:n.*33_*40del
NM_001185078.2:c.*33_*40del NP_001172007.1:n.*33_*40del
NM_001301240.1:c.502+146_502+153del NP_001288169.1:n.502+146_502+153del
NM_001301241.1:c.502+146_502+153del NP_001288170.1:n.502+146_502+153del
NM_001301242.1:c.536_543del NP_001288171.1:p.Gly179AspfsTer19
NM_001301243.1:c.*33_*40del NP_001288172.1:n.*33_*40del
NM_004309.5:c.*33_*40del NP_004300.1:n.*33_*40del
NR_125441.1:n.707_714del
XM_011523574.1:c.*33_*40del XP_011521876.1:n.*33_*40del
NM_004309.6:c.*33_*40del MANE Select NP_004300.1:n.*33_*40del
NM_001185077.3:c.*33_*40del NP_001172006.1:n.*33_*40del
NM_001185078.3:c.*33_*40del NP_001172007.1:n.*33_*40del
NM_001301240.2:c.502+146_502+153del NP_001288169.1:n.502+146_502+153del
NM_001301241.2:c.502+146_502+153del NP_001288170.1:n.502+146_502+153del
NM_001301242.2:c.536_543del NP_001288171.1:p.Gly179AspfsTer19
NM_001301243.2:c.*33_*40del NP_001288172.1:n.*33_*40del
NR_125441.2:n.638_645del