Canonical Allele Identifier: CA342634986

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557708C>A (hg19) ; chr1:g.154585232C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154585232C>A , CM000663.2:g.154585232C>A	GRCh38
NC_000001.10:g.154557708C>A , CM000663.1:g.154557708C>A	GRCh37
NC_000001.9:g.152824332C>A	NCBI36
NG_011844.1:g.47730G>T
NG_011844.2:g.51329G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3322G>T	ENSP00000497790.2:n.3322G>T
ENST00000649724.2:c.3458G>T	ENSP00000497932.2:p.Arg1153Ile
ENST00000680270.2:c.3311G>T	ENSP00000505532.2:p.Arg1104Ile
ENST00000681056.2:c.3080G>T	ENSP00000506234.2:p.Arg1027Ile
ENST00000368471.8:c.2543G>T	ENSP00000357456.3:p.Arg848Ile
ENST00000368474.9:c.3428G>T MANE Select	ENSP00000357459.4:p.Arg1143Ile
ENST00000492630.2:n.2221G>T
ENST00000529168.2:c.3350G>T	ENSP00000431794.2:p.Arg1117Ile
ENST00000647682.2:n.3413G>T
ENST00000648231.2:c.2543G>T	ENSP00000497555.1:p.Arg848Ile
ENST00000648311.1:c.2543G>T	ENSP00000498137.1:p.Arg848Ile
ENST00000648714.2:c.*903G>T	ENSP00000497434.2:n.*903G>T
ENST00000649021.1:n.4164G>T
ENST00000649022.2:c.2543G>T	ENSP00000496896.2:p.Arg848Ile
ENST00000649042.1:c.2543G>T	ENSP00000497790.1:p.Arg848Ile
ENST00000649408.2:c.*594G>T	ENSP00000497386.2:n.*594G>T
ENST00000649724.1:c.2543G>T	ENSP00000497932.1:p.Arg848Ile
ENST00000649749.1:c.2543G>T	ENSP00000497210.1:p.Arg848Ile
ENST00000679375.1:c.*1660G>T	ENSP00000505887.1:n.*1660G>T
ENST00000679465.1:n.4289G>T
ENST00000679805.1:n.4164G>T
ENST00000679899.1:c.2486G>T	ENSP00000505996.1:p.Arg829Ile
ENST00000680270.1:c.2543G>T	ENSP00000505532.1:p.Arg848Ile
ENST00000680305.1:c.3245G>T	ENSP00000506312.1:p.Arg1082Ile
ENST00000681056.1:c.2543G>T	ENSP00000506234.1:p.Arg848Ile
ENST00000681235.1:c.*2950G>T	ENSP00000506606.1:n.*2950G>T
ENST00000681429.1:n.3096G>T
ENST00000681683.1:c.2543G>T	ENSP00000506666.1:p.Arg848Ile
ENST00000681786.1:n.4289G>T
ENST00000681901.1:c.*3028G>T	ENSP00000504883.1:n.*3028G>T
ENST00000368471.7:c.2543G>T	ENSP00000357456.3:p.Arg848Ile
ENST00000368474.8:c.3428G>T	ENSP00000357459.4:p.Arg1143Ile
ENST00000492630.1:n.187G>T
ENST00000529168.1:c.3335G>T	ENSP00000431794.1:p.Arg1112Ile
NM_001025107.2:c.2543G>T	NP_001020278.1:p.Arg848Ile
NM_001111.4:c.3428G>T	NP_001102.2:p.Arg1143Ile
NM_001193495.1:c.2543G>T	NP_001180424.1:p.Arg848Ile
NM_015840.3:c.3350G>T	NP_056655.2:p.Arg1117Ile
NM_015841.3:c.3293G>T	NP_056656.2:p.Arg1098Ile
XM_006711109.1:c.3458G>T	XP_006711172.1:p.Arg1153Ile
XM_006711111.2:c.2543G>T	XP_006711174.1:p.Arg848Ile
XM_006711112.1:c.2543G>T	XP_006711175.1:p.Arg848Ile
XM_006711113.1:c.2543G>T	XP_006711176.1:p.Arg848Ile
XM_011509060.1:c.3557G>T	XP_011507362.1:p.Arg1186Ile
XM_011509061.1:c.3479G>T	XP_011507363.1:p.Arg1160Ile
XM_011509062.1:c.3446G>T	XP_011507364.1:p.Arg1149Ile
NM_001025107.3:c.2543G>T	NP_001020278.1:p.Arg848Ile
NM_001111.5:c.3428G>T MANE Select	NP_001102.3:p.Arg1143Ile
NM_001193495.2:c.2543G>T	NP_001180424.1:p.Arg848Ile
NM_001365045.1:c.3455G>T	NP_001351974.1:p.Arg1152Ile
NM_001365046.1:c.2543G>T	NP_001351975.1:p.Arg848Ile
NM_001365047.1:c.2543G>T	NP_001351976.1:p.Arg848Ile
NM_001365048.1:c.2543G>T	NP_001351977.1:p.Arg848Ile
NM_001365049.1:c.2465G>T	NP_001351978.1:p.Arg822Ile
NM_015840.4:c.3350G>T	NP_056655.3:p.Arg1117Ile
NM_015841.4:c.3293G>T	NP_056656.3:p.Arg1098Ile
XM_006711113.2:c.2543G>T	XP_006711176.1:p.Arg848Ile
XM_011509061.2:c.2465G>T	XP_011507363.2:p.Arg822Ile
XM_024449674.1:c.3557G>T	XP_024305442.1:p.Arg1186Ile