Canonical Allele Identifier: CA656896013

Gene: ARHGDIA

Linked Data

• COSMIC: COSN20084036

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868813_81868814insA , CM000679.2:g.81868813_81868814insA	GRCh38
NC_000017.10:g.79826689_79826690insA , CM000679.1:g.79826689_79826690insA	GRCh37
NC_000017.9:g.77419978_77419979insA	NCBI36
NG_034210.1:g.7593_7594insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.*62_*63insT MANE Select	ENSP00000269321.7:n.*62_*63insT
ENST00000269321.11:c.*62_*63insT	ENSP00000269321.7:n.*62_*63insT
ENST00000400721.8:c.*62_*63insT	ENSP00000383556.4:n.*62_*63insT
ENST00000541078.6:c.*62_*63insT	ENSP00000441348.2:n.*62_*63insT
ENST00000579121.5:c.502+175_502+176insT	ENSP00000462960.1:n.502+175_502+176insT
ENST00000580685.5:c.*62_*63insT	ENSP00000464205.1:n.*62_*63insT
ENST00000581876.5:c.*62_*63insT	ENSP00000461956.1:n.*62_*63insT
ENST00000583868.5:c.565_566insT	ENSP00000462209.1:p.Pro189LeufsTer12
ENST00000584461.5:c.502+175_502+176insT	ENSP00000463939.1:n.502+175_502+176insT
NM_001185077.2:c.*62_*63insT	NP_001172006.1:n.*62_*63insT
NM_001185078.2:c.*62_*63insT	NP_001172007.1:n.*62_*63insT
NM_001301240.1:c.502+175_502+176insT	NP_001288169.1:n.502+175_502+176insT
NM_001301241.1:c.502+175_502+176insT	NP_001288170.1:n.502+175_502+176insT
NM_001301242.1:c.565_566insT	NP_001288171.1:p.Pro189LeufsTer12
NM_001301243.1:c.*62_*63insT	NP_001288172.1:n.*62_*63insT
NM_004309.5:c.*62_*63insT	NP_004300.1:n.*62_*63insT
NR_125441.1:n.736_737insT
XM_011523574.1:c.*62_*63insT	XP_011521876.1:n.*62_*63insT
NM_004309.6:c.*62_*63insT MANE Select	NP_004300.1:n.*62_*63insT
NM_001185077.3:c.*62_*63insT	NP_001172006.1:n.*62_*63insT
NM_001185078.3:c.*62_*63insT	NP_001172007.1:n.*62_*63insT
NM_001301240.2:c.502+175_502+176insT	NP_001288169.1:n.502+175_502+176insT
NM_001301241.2:c.502+175_502+176insT	NP_001288170.1:n.502+175_502+176insT
NM_001301242.2:c.565_566insT	NP_001288171.1:p.Pro189LeufsTer12
NM_001301243.2:c.*62_*63insT	NP_001288172.1:n.*62_*63insT
NR_125441.2:n.667_668insT