Canonical Allele Identifier: CA342597260

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154601453A>T , CM000663.2:g.154601453A>T	GRCh38
NC_000001.10:g.154573929A>T , CM000663.1:g.154573929A>T	GRCh37
NC_000001.9:g.152840553A>T	NCBI36
NG_011844.1:g.31509T>A
NG_011844.2:g.35108T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001111.5:c.1189T>A MANE Select	NP_001102.3:p.Ser397Thr
ENST00000368474.9:c.1189T>A MANE Select	ENSP00000357459.4:p.Ser397Thr
NM_001025107.2:c.304T>A	NP_001020278.1:p.Ser102Thr
NM_001025107.3:c.304T>A	NP_001020278.1:p.Ser102Thr
NM_001111.4:c.1189T>A	NP_001102.2:p.Ser397Thr
NM_001193495.1:c.304T>A	NP_001180424.1:p.Ser102Thr
NM_001193495.2:c.304T>A	NP_001180424.1:p.Ser102Thr
NM_001365045.1:c.1216T>A	NP_001351974.1:p.Ser406Thr
NM_001365046.1:c.304T>A	NP_001351975.1:p.Ser102Thr
NM_001365047.1:c.304T>A	NP_001351976.1:p.Ser102Thr
NM_001365048.1:c.304T>A	NP_001351977.1:p.Ser102Thr
NM_001365049.1:c.304T>A	NP_001351978.1:p.Ser102Thr
NM_015840.3:c.1189T>A	NP_056655.2:p.Ser397Thr
NM_015840.4:c.1189T>A	NP_056655.3:p.Ser397Thr
NM_015841.3:c.1189T>A	NP_056656.2:p.Ser397Thr
NM_015841.4:c.1189T>A	NP_056656.3:p.Ser397Thr
ENST00000368471.7:c.304T>A	ENSP00000357456.3:p.Ser102Thr
ENST00000368471.8:c.304T>A	ENSP00000357456.3:p.Ser102Thr
ENST00000368474.8:c.1189T>A	ENSP00000357459.4:p.Ser397Thr
ENST00000463920.5:n.1071T>A
ENST00000529168.1:c.1174T>A	ENSP00000431794.1:p.Ser392Thr
ENST00000529168.2:c.1189T>A	ENSP00000431794.2:p.Ser397Thr
ENST00000647682.2:n.919T>A
ENST00000648231.2:c.304T>A	ENSP00000497555.1:p.Ser102Thr
ENST00000648311.1:c.304T>A	ENSP00000498137.1:p.Ser102Thr
ENST00000648714.2:c.1189T>A	ENSP00000497434.2:p.Ser397Thr
ENST00000648871.1:c.304T>A	ENSP00000497793.1:p.Ser102Thr
ENST00000649021.1:n.1225T>A
ENST00000649022.2:c.304T>A	ENSP00000496896.2:p.Ser102Thr
ENST00000649042.1:c.304T>A	ENSP00000497790.1:p.Ser102Thr
ENST00000649042.2:c.1083T>A	ENSP00000497790.2:n.1083T>A
ENST00000649408.2:c.1189T>A	ENSP00000497386.2:p.Ser397Thr
ENST00000649724.1:c.304T>A	ENSP00000497932.1:p.Ser102Thr
ENST00000649724.2:c.1219T>A	ENSP00000497932.2:p.Ser407Thr
ENST00000649749.1:c.304T>A	ENSP00000497210.1:p.Ser102Thr
ENST00000679375.1:c.304T>A	ENSP00000505887.1:p.Ser102Thr
ENST00000679465.1:n.1387T>A
ENST00000679805.1:n.1225T>A
ENST00000679899.1:c.304T>A	ENSP00000505996.1:p.Ser102Thr
ENST00000680270.1:c.304T>A	ENSP00000505532.1:p.Ser102Thr
ENST00000680270.2:c.1072T>A	ENSP00000505532.2:p.Ser358Thr
ENST00000680305.1:c.1189T>A	ENSP00000506312.1:p.Ser397Thr
ENST00000680472.1:n.1228T>A
ENST00000681056.1:c.304T>A	ENSP00000506234.1:p.Ser102Thr
ENST00000681056.2:c.841T>A	ENSP00000506234.2:p.Ser281Thr
ENST00000681235.1:c.*789T>A	ENSP00000506606.1:n.*789T>A
ENST00000681683.1:c.304T>A	ENSP00000506666.1:p.Ser102Thr
ENST00000681786.1:n.1387T>A
ENST00000681901.1:c.*789T>A	ENSP00000504883.1:n.*789T>A
XM_006711109.1:c.1219T>A	XP_006711172.1:p.Ser407Thr
XM_006711111.2:c.304T>A	XP_006711174.1:p.Ser102Thr
XM_006711112.1:c.304T>A	XP_006711175.1:p.Ser102Thr
XM_006711113.1:c.304T>A	XP_006711176.1:p.Ser102Thr
XM_006711113.2:c.304T>A	XP_006711176.1:p.Ser102Thr
XM_011509060.1:c.1318T>A	XP_011507362.1:p.Ser440Thr
XM_011509061.1:c.1318T>A	XP_011507363.1:p.Ser440Thr
XM_011509061.2:c.304T>A	XP_011507363.2:p.Ser102Thr
XM_011509062.1:c.1207T>A	XP_011507364.1:p.Ser403Thr
XM_024449674.1:c.1318T>A	XP_024305442.1:p.Ser440Thr