Canonical Allele Identifier: CA342599577

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154601763A>T , CM000663.2:g.154601763A>T	GRCh38
NC_000001.10:g.154574239A>T , CM000663.1:g.154574239A>T	GRCh37
NC_000001.9:g.152840863A>T	NCBI36
NG_011844.1:g.31199T>A
NG_011844.2:g.34798T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001111.5:c.879T>A MANE Select	NP_001102.3:p.Phe293Leu
ENST00000368474.9:c.879T>A MANE Select	ENSP00000357459.4:p.Phe293Leu
NM_001025107.2:c.-7T>A	NP_001020278.1:n.-7T>A
NM_001025107.3:c.-7T>A	NP_001020278.1:n.-7T>A
NM_001111.4:c.879T>A	NP_001102.2:p.Phe293Leu
NM_001193495.1:c.-7T>A	NP_001180424.1:n.-7T>A
NM_001193495.2:c.-7T>A	NP_001180424.1:n.-7T>A
NM_001365045.1:c.906T>A	NP_001351974.1:p.Phe302Leu
NM_001365046.1:c.-7T>A	NP_001351975.1:n.-7T>A
NM_001365047.1:c.-7T>A	NP_001351976.1:n.-7T>A
NM_001365048.1:c.-7T>A	NP_001351977.1:n.-7T>A
NM_001365049.1:c.-7T>A	NP_001351978.1:n.-7T>A
NM_015840.3:c.879T>A	NP_056655.2:p.Phe293Leu
NM_015840.4:c.879T>A	NP_056655.3:p.Phe293Leu
NM_015841.3:c.879T>A	NP_056656.2:p.Phe293Leu
NM_015841.4:c.879T>A	NP_056656.3:p.Phe293Leu
ENST00000368471.7:c.-7T>A	ENSP00000357456.3:n.-7T>A
ENST00000368471.8:c.-7T>A	ENSP00000357456.3:n.-7T>A
ENST00000368474.8:c.879T>A	ENSP00000357459.4:p.Phe293Leu
ENST00000463920.5:n.761T>A
ENST00000529168.1:c.864T>A	ENSP00000431794.1:p.Phe288Leu
ENST00000529168.2:c.879T>A	ENSP00000431794.2:p.Phe293Leu
ENST00000647682.2:n.609T>A
ENST00000648231.2:c.-7T>A	ENSP00000497555.1:n.-7T>A
ENST00000648311.1:c.-7T>A	ENSP00000498137.1:n.-7T>A
ENST00000648714.2:c.879T>A	ENSP00000497434.2:p.Phe293Leu
ENST00000648871.1:c.-7T>A	ENSP00000497793.1:n.-7T>A
ENST00000649021.1:n.915T>A
ENST00000649022.2:c.-7T>A	ENSP00000496896.2:n.-7T>A
ENST00000649042.1:c.-7T>A	ENSP00000497790.1:n.-7T>A
ENST00000649042.2:c.773T>A	ENSP00000497790.2:n.773T>A
ENST00000649408.2:c.879T>A	ENSP00000497386.2:p.Phe293Leu
ENST00000649724.1:c.-7T>A	ENSP00000497932.1:n.-7T>A
ENST00000649724.2:c.909T>A	ENSP00000497932.2:p.Phe303Leu
ENST00000649749.1:c.-7T>A	ENSP00000497210.1:n.-7T>A
ENST00000679375.1:c.-7T>A	ENSP00000505887.1:n.-7T>A
ENST00000679465.1:n.1077T>A
ENST00000679805.1:n.915T>A
ENST00000679899.1:c.-7T>A	ENSP00000505996.1:n.-7T>A
ENST00000680270.1:c.-7T>A	ENSP00000505532.1:n.-7T>A
ENST00000680270.2:c.762T>A	ENSP00000505532.2:p.Phe254Leu
ENST00000680305.1:c.879T>A	ENSP00000506312.1:p.Phe293Leu
ENST00000680472.1:n.918T>A
ENST00000681056.1:c.-7T>A	ENSP00000506234.1:n.-7T>A
ENST00000681056.2:c.531T>A	ENSP00000506234.2:p.Phe177Leu
ENST00000681235.1:c.*479T>A	ENSP00000506606.1:n.*479T>A
ENST00000681683.1:c.-7T>A	ENSP00000506666.1:n.-7T>A
ENST00000681786.1:n.1077T>A
ENST00000681901.1:c.*479T>A	ENSP00000504883.1:n.*479T>A
XM_006711109.1:c.909T>A	XP_006711172.1:p.Phe303Leu
XM_006711111.2:c.-7T>A	XP_006711174.1:n.-7T>A
XM_006711112.1:c.-7T>A	XP_006711175.1:n.-7T>A
XM_006711113.1:c.-7T>A	XP_006711176.1:n.-7T>A
XM_006711113.2:c.-7T>A	XP_006711176.1:n.-7T>A
XM_011509060.1:c.1008T>A	XP_011507362.1:p.Phe336Leu
XM_011509061.1:c.1008T>A	XP_011507363.1:p.Phe336Leu
XM_011509061.2:c.-7T>A	XP_011507363.2:n.-7T>A
XM_011509062.1:c.897T>A	XP_011507364.1:p.Phe299Leu
XM_024449674.1:c.1008T>A	XP_024305442.1:p.Phe336Leu