Canonical Allele Identifier: CA986873058

Gene: ARHGDIA

Linked Data

• gnomAD v3: 17-81868860-C-CCGGGGCCCCACTCACTCTTGA
• gnomAD v4: 17-81868860-C-CCGGGGCCCCACTCACTCTTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868862_81868863insGGGCCCCACTCACTCTTGACG , CM000679.2:g.81868862_81868863insGGGCCCCACTCACTCTTGACG	GRCh38
NC_000017.10:g.79826738_79826739insGGGCCCCACTCACTCTTGACG , CM000679.1:g.79826738_79826739insGGGCCCCACTCACTCTTGACG	GRCh37
NC_000017.9:g.77420027_77420028insGGGCCCCACTCACTCTTGACG	NCBI36
NG_034210.1:g.7546_7547insTCAAGAGTGAGTGGGGCCCCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG MANE Select	ENSP00000269321.7:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
ENST00000269321.11:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	ENSP00000269321.7:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
ENST00000400721.8:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	ENSP00000383556.4:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
ENST00000541078.6:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	ENSP00000441348.2:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
ENST00000579121.5:c.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG	ENSP00000462960.1:n.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG
ENST00000580685.5:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	ENSP00000464205.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
ENST00000581876.5:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	ENSP00000461956.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
ENST00000583868.5:c.518_519insTCAAGAGTGAGTGGGGCCCCG	ENSP00000462209.1:p.Arg174GlnfsTer3
ENST00000584461.5:c.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG	ENSP00000463939.1:n.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG
NM_001185077.2:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	NP_001172006.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NM_001185078.2:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	NP_001172007.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NM_001301240.1:c.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG	NP_001288169.1:n.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG
NM_001301241.1:c.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG	NP_001288170.1:n.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG
NM_001301242.1:c.518_519insTCAAGAGTGAGTGGGGCCCCG	NP_001288171.1:p.Arg174GlnfsTer3
NM_001301243.1:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	NP_001288172.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NM_004309.5:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	NP_004300.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NR_125441.1:n.689_690insTCAAGAGTGAGTGGGGCCCCG
XM_011523574.1:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	XP_011521876.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NM_004309.6:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG MANE Select	NP_004300.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NM_001185077.3:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	NP_001172006.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NM_001185078.3:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	NP_001172007.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NM_001301240.2:c.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG	NP_001288169.1:n.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG
NM_001301241.2:c.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG	NP_001288170.1:n.502+128_502+129insTCAAGAGTGAGTGGGGCCCCG
NM_001301242.2:c.518_519insTCAAGAGTGAGTGGGGCCCCG	NP_001288171.1:p.Arg174GlnfsTer3
NM_001301243.2:c.*15_*16insTCAAGAGTGAGTGGGGCCCCG	NP_001288172.1:n.*15_*16insTCAAGAGTGAGTGGGGCCCCG
NR_125441.2:n.620_621insTCAAGAGTGAGTGGGGCCCCG