Canonical Allele Identifier: CA656896016

Gene: ARHGDIA

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868861_81868862insT , CM000679.2:g.81868861_81868862insT	GRCh38
NC_000017.10:g.79826737_79826738insT , CM000679.1:g.79826737_79826738insT	GRCh37
NC_000017.9:g.77420026_77420027insT	NCBI36
NG_034210.1:g.7545_7546insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.*14_*15insA MANE Select	ENSP00000269321.7:n.*14_*15insA
ENST00000269321.11:c.*14_*15insA	ENSP00000269321.7:n.*14_*15insA
ENST00000400721.8:c.*14_*15insA	ENSP00000383556.4:n.*14_*15insA
ENST00000541078.6:c.*14_*15insA	ENSP00000441348.2:n.*14_*15insA
ENST00000579121.5:c.502+127_502+128insA	ENSP00000462960.1:n.502+127_502+128insA
ENST00000580685.5:c.*14_*15insA	ENSP00000464205.1:n.*14_*15insA
ENST00000581876.5:c.*14_*15insA	ENSP00000461956.1:n.*14_*15insA
ENST00000583868.5:c.517_518insA	ENSP00000462209.1:p.Arg173GlnfsTer6
ENST00000584461.5:c.502+127_502+128insA	ENSP00000463939.1:n.502+127_502+128insA
NM_001185077.2:c.*14_*15insA	NP_001172006.1:n.*14_*15insA
NM_001185078.2:c.*14_*15insA	NP_001172007.1:n.*14_*15insA
NM_001301240.1:c.502+127_502+128insA	NP_001288169.1:n.502+127_502+128insA
NM_001301241.1:c.502+127_502+128insA	NP_001288170.1:n.502+127_502+128insA
NM_001301242.1:c.517_518insA	NP_001288171.1:p.Arg173GlnfsTer6
NM_001301243.1:c.*14_*15insA	NP_001288172.1:n.*14_*15insA
NM_004309.5:c.*14_*15insA	NP_004300.1:n.*14_*15insA
NR_125441.1:n.688_689insA
XM_011523574.1:c.*14_*15insA	XP_011521876.1:n.*14_*15insA
NM_004309.6:c.*14_*15insA MANE Select	NP_004300.1:n.*14_*15insA
NM_001185077.3:c.*14_*15insA	NP_001172006.1:n.*14_*15insA
NM_001185078.3:c.*14_*15insA	NP_001172007.1:n.*14_*15insA
NM_001301240.2:c.502+127_502+128insA	NP_001288169.1:n.502+127_502+128insA
NM_001301241.2:c.502+127_502+128insA	NP_001288170.1:n.502+127_502+128insA
NM_001301242.2:c.517_518insA	NP_001288171.1:p.Arg173GlnfsTer6
NM_001301243.2:c.*14_*15insA	NP_001288172.1:n.*14_*15insA
NR_125441.2:n.619_620insA