Canonical Allele Identifier: CA1131695

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154602155C>T , CM000663.2:g.154602155C>T	GRCh38
NC_000001.10:g.154574631C>T , CM000663.1:g.154574631C>T	GRCh37
NC_000001.9:g.152841255C>T	NCBI36
NG_011844.1:g.30807G>A
NG_011844.2:g.34406G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001111.5:c.487G>A MANE Select	NP_001102.3:p.Gly163Arg
ENST00000368474.9:c.487G>A MANE Select	ENSP00000357459.4:p.Gly163Arg
NM_001025107.2:c.-399G>A	NP_001020278.1:n.-399G>A
NM_001025107.3:c.-399G>A	NP_001020278.1:n.-399G>A
NM_001111.4:c.487G>A	NP_001102.2:p.Gly163Arg
NM_001193495.1:c.-399G>A	NP_001180424.1:n.-399G>A
NM_001193495.2:c.-399G>A	NP_001180424.1:n.-399G>A
NM_001365045.1:c.514G>A	NP_001351974.1:p.Gly172Arg
NM_001365046.1:c.-399G>A	NP_001351975.1:n.-399G>A
NM_001365047.1:c.-399G>A	NP_001351976.1:n.-399G>A
NM_001365048.1:c.-399G>A	NP_001351977.1:n.-399G>A
NM_001365049.1:c.-399G>A	NP_001351978.1:n.-399G>A
NM_015840.3:c.487G>A	NP_056655.2:p.Gly163Arg
NM_015840.4:c.487G>A	NP_056655.3:p.Gly163Arg
NM_015841.3:c.487G>A	NP_056656.2:p.Gly163Arg
NM_015841.4:c.487G>A	NP_056656.3:p.Gly163Arg
ENST00000368471.7:c.-399G>A	ENSP00000357456.3:n.-399G>A
ENST00000368471.8:c.-399G>A	ENSP00000357456.3:n.-399G>A
ENST00000368474.8:c.487G>A	ENSP00000357459.4:p.Gly163Arg
ENST00000463920.5:n.369G>A
ENST00000471068.1:n.518G>A
ENST00000471068.2:n.484G>A
ENST00000494866.1:n.394G>A
ENST00000529168.1:c.472G>A	ENSP00000431794.1:p.Gly158Arg
ENST00000529168.2:c.487G>A	ENSP00000431794.2:p.Gly163Arg
ENST00000647682.2:n.217G>A
ENST00000648231.2:c.-399G>A	ENSP00000497555.1:n.-399G>A
ENST00000648311.1:c.-399G>A	ENSP00000498137.1:n.-399G>A
ENST00000648714.2:c.487G>A	ENSP00000497434.2:p.Gly163Arg
ENST00000648871.1:c.-399G>A	ENSP00000497793.1:n.-399G>A
ENST00000649021.1:n.523G>A
ENST00000649022.2:c.-399G>A	ENSP00000496896.2:n.-399G>A
ENST00000649042.1:c.-399G>A	ENSP00000497790.1:n.-399G>A
ENST00000649042.2:c.381G>A	ENSP00000497790.2:n.381G>A
ENST00000649408.2:c.487G>A	ENSP00000497386.2:p.Gly163Arg
ENST00000649724.1:c.-399G>A	ENSP00000497932.1:n.-399G>A
ENST00000649724.2:c.517G>A	ENSP00000497932.2:p.Gly173Arg
ENST00000649749.1:c.-399G>A	ENSP00000497210.1:n.-399G>A
ENST00000679375.1:c.-399G>A	ENSP00000505887.1:n.-399G>A
ENST00000679465.1:n.685G>A
ENST00000679805.1:n.523G>A
ENST00000679899.1:c.-399G>A	ENSP00000505996.1:n.-399G>A
ENST00000680270.1:c.-252G>A	ENSP00000505532.1:n.-252G>A
ENST00000680270.2:c.517G>A	ENSP00000505532.2:p.Gly173Arg
ENST00000680305.1:c.487G>A	ENSP00000506312.1:p.Gly163Arg
ENST00000680472.1:n.526G>A
ENST00000681056.1:c.-399G>A	ENSP00000506234.1:n.-399G>A
ENST00000681056.2:c.139G>A	ENSP00000506234.2:p.Gly47Arg
ENST00000681235.1:c.*87G>A	ENSP00000506606.1:n.*87G>A
ENST00000681683.1:c.-399G>A	ENSP00000506666.1:n.-399G>A
ENST00000681786.1:n.685G>A
ENST00000681901.1:c.*87G>A	ENSP00000504883.1:n.*87G>A
XM_006711109.1:c.517G>A	XP_006711172.1:p.Gly173Arg
XM_006711111.2:c.-399G>A	XP_006711174.1:n.-399G>A
XM_006711112.1:c.-399G>A	XP_006711175.1:n.-399G>A
XM_006711113.1:c.-399G>A	XP_006711176.1:n.-399G>A
XM_006711113.2:c.-399G>A	XP_006711176.1:n.-399G>A
XM_011509060.1:c.616G>A	XP_011507362.1:p.Gly206Arg
XM_011509061.1:c.616G>A	XP_011507363.1:p.Gly206Arg
XM_011509061.2:c.-399G>A	XP_011507363.2:n.-399G>A
XM_011509062.1:c.505G>A	XP_011507364.1:p.Gly169Arg
XM_024449674.1:c.616G>A	XP_024305442.1:p.Gly206Arg