Canonical Allele Identifier: CA342635431

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154585836G>A , CM000663.2:g.154585836G>A	GRCh38
NC_000001.10:g.154558312G>A , CM000663.1:g.154558312G>A	GRCh37
NC_000001.9:g.152824936G>A	NCBI36
NG_011844.1:g.47126C>T
NG_011844.2:g.50725C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001111.5:c.3232C>T MANE Select	NP_001102.3:p.Arg1078Cys
ENST00000368474.9:c.3232C>T MANE Select	ENSP00000357459.4:p.Arg1078Cys
NM_001025107.2:c.2347C>T	NP_001020278.1:p.Arg783Cys
NM_001025107.3:c.2347C>T	NP_001020278.1:p.Arg783Cys
NM_001111.4:c.3232C>T	NP_001102.2:p.Arg1078Cys
NM_001193495.1:c.2347C>T	NP_001180424.1:p.Arg783Cys
NM_001193495.2:c.2347C>T	NP_001180424.1:p.Arg783Cys
NM_001365045.1:c.3259C>T	NP_001351974.1:p.Arg1087Cys
NM_001365046.1:c.2347C>T	NP_001351975.1:p.Arg783Cys
NM_001365047.1:c.2347C>T	NP_001351976.1:p.Arg783Cys
NM_001365048.1:c.2347C>T	NP_001351977.1:p.Arg783Cys
NM_001365049.1:c.2269C>T	NP_001351978.1:p.Arg757Cys
NM_015840.3:c.3154C>T	NP_056655.2:p.Arg1052Cys
NM_015840.4:c.3154C>T	NP_056655.3:p.Arg1052Cys
NM_015841.3:c.3097C>T	NP_056656.2:p.Arg1033Cys
NM_015841.4:c.3097C>T	NP_056656.3:p.Arg1033Cys
ENST00000368471.7:c.2347C>T	ENSP00000357456.3:p.Arg783Cys
ENST00000368471.8:c.2347C>T	ENSP00000357456.3:p.Arg783Cys
ENST00000368474.8:c.3232C>T	ENSP00000357459.4:p.Arg1078Cys
ENST00000492630.2:n.1617C>T
ENST00000529168.1:c.3139C>T	ENSP00000431794.1:p.Arg1047Cys
ENST00000529168.2:c.3154C>T	ENSP00000431794.2:p.Arg1052Cys
ENST00000530954.1:n.369C>T
ENST00000647682.2:n.3217C>T
ENST00000648231.2:c.2347C>T	ENSP00000497555.1:p.Arg783Cys
ENST00000648311.1:c.2347C>T	ENSP00000498137.1:p.Arg783Cys
ENST00000648714.2:c.*707C>T	ENSP00000497434.2:n.*707C>T
ENST00000649021.1:n.3560C>T
ENST00000649022.2:c.2347C>T	ENSP00000496896.2:p.Arg783Cys
ENST00000649042.1:c.2347C>T	ENSP00000497790.1:p.Arg783Cys
ENST00000649042.2:c.3126C>T	ENSP00000497790.2:n.3126C>T
ENST00000649408.2:c.*398C>T	ENSP00000497386.2:n.*398C>T
ENST00000649724.1:c.2347C>T	ENSP00000497932.1:p.Arg783Cys
ENST00000649724.2:c.3262C>T	ENSP00000497932.2:p.Arg1088Cys
ENST00000649749.1:c.2347C>T	ENSP00000497210.1:p.Arg783Cys
ENST00000679375.1:c.*1464C>T	ENSP00000505887.1:n.*1464C>T
ENST00000679465.1:n.3685C>T
ENST00000679805.1:n.3560C>T
ENST00000679899.1:c.2290C>T	ENSP00000505996.1:p.Arg764Cys
ENST00000680270.1:c.2347C>T	ENSP00000505532.1:p.Arg783Cys
ENST00000680270.2:c.3115C>T	ENSP00000505532.2:p.Arg1039Cys
ENST00000680305.1:c.3049C>T	ENSP00000506312.1:p.Arg1017Cys
ENST00000681056.1:c.2347C>T	ENSP00000506234.1:p.Arg783Cys
ENST00000681056.2:c.2884C>T	ENSP00000506234.2:p.Arg962Cys
ENST00000681235.1:c.*2754C>T	ENSP00000506606.1:n.*2754C>T
ENST00000681429.1:n.2492C>T
ENST00000681683.1:c.2347C>T	ENSP00000506666.1:p.Arg783Cys
ENST00000681786.1:n.3685C>T
ENST00000681901.1:c.*2832C>T	ENSP00000504883.1:n.*2832C>T
XM_006711109.1:c.3262C>T	XP_006711172.1:p.Arg1088Cys
XM_006711111.2:c.2347C>T	XP_006711174.1:p.Arg783Cys
XM_006711112.1:c.2347C>T	XP_006711175.1:p.Arg783Cys
XM_006711113.1:c.2347C>T	XP_006711176.1:p.Arg783Cys
XM_006711113.2:c.2347C>T	XP_006711176.1:p.Arg783Cys
XM_011509060.1:c.3361C>T	XP_011507362.1:p.Arg1121Cys
XM_011509061.1:c.3283C>T	XP_011507363.1:p.Arg1095Cys
XM_011509061.2:c.2269C>T	XP_011507363.2:p.Arg757Cys
XM_011509062.1:c.3250C>T	XP_011507364.1:p.Arg1084Cys
XM_024449674.1:c.3361C>T	XP_024305442.1:p.Arg1121Cys