Canonical Allele Identifier: CA2640522749

Gene: ARHGDIA

Linked Data

• gnomAD v4: 17-81868809-CTGGGGGGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868810_81868817del , CM000679.2:g.81868810_81868817del	GRCh38
NC_000017.10:g.79826686_79826693del , CM000679.1:g.79826686_79826693del	GRCh37
NC_000017.9:g.77419975_77419982del	NCBI36
NG_034210.1:g.7590_7597del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.*59_*66del MANE Select	ENSP00000269321.7:n.*59_*66del
ENST00000269321.11:c.*59_*66del	ENSP00000269321.7:n.*59_*66del
ENST00000400721.8:c.*59_*66del	ENSP00000383556.4:n.*59_*66del
ENST00000541078.6:c.*59_*66del	ENSP00000441348.2:n.*59_*66del
ENST00000579121.5:c.502+172_502+179del	ENSP00000462960.1:n.502+172_502+179del
ENST00000580685.5:c.*59_*66del	ENSP00000464205.1:n.*59_*66del
ENST00000581876.5:c.*59_*66del	ENSP00000461956.1:n.*59_*66del
ENST00000583868.5:c.562_569del	ENSP00000462209.1:p.Pro188AlafsTer10
ENST00000584461.5:c.502+172_502+179del	ENSP00000463939.1:n.502+172_502+179del
NM_001185077.2:c.*59_*66del	NP_001172006.1:n.*59_*66del
NM_001185078.2:c.*59_*66del	NP_001172007.1:n.*59_*66del
NM_001301240.1:c.502+172_502+179del	NP_001288169.1:n.502+172_502+179del
NM_001301241.1:c.502+172_502+179del	NP_001288170.1:n.502+172_502+179del
NM_001301242.1:c.562_569del	NP_001288171.1:p.Pro188AlafsTer10
NM_001301243.1:c.*59_*66del	NP_001288172.1:n.*59_*66del
NM_004309.5:c.*59_*66del	NP_004300.1:n.*59_*66del
NR_125441.1:n.733_740del
XM_011523574.1:c.*59_*66del	XP_011521876.1:n.*59_*66del
NM_004309.6:c.*59_*66del MANE Select	NP_004300.1:n.*59_*66del
NM_001185077.3:c.*59_*66del	NP_001172006.1:n.*59_*66del
NM_001185078.3:c.*59_*66del	NP_001172007.1:n.*59_*66del
NM_001301240.2:c.502+172_502+179del	NP_001288169.1:n.502+172_502+179del
NM_001301241.2:c.502+172_502+179del	NP_001288170.1:n.502+172_502+179del
NM_001301242.2:c.562_569del	NP_001288171.1:p.Pro188AlafsTer10
NM_001301243.2:c.*59_*66del	NP_001288172.1:n.*59_*66del
NR_125441.2:n.664_671del