Canonical Allele Identifier: CA342634468

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557309T>A (hg19) ; chr1:g.154584833T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584833T>A , CM000663.2:g.154584833T>A	GRCh38
NC_000001.10:g.154557309T>A , CM000663.1:g.154557309T>A	GRCh37
NC_000001.9:g.152823933T>A	NCBI36
NG_011844.1:g.48129A>T
NG_011844.2:g.51728A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3548A>T	ENSP00000497790.2:n.3548A>T
ENST00000649724.2:c.3684A>T	ENSP00000497932.2:p.Glu1228Asp
ENST00000680270.2:c.3537A>T	ENSP00000505532.2:p.Glu1179Asp
ENST00000681056.2:c.3306A>T	ENSP00000506234.2:p.Glu1102Asp
ENST00000368471.8:c.2769A>T	ENSP00000357456.3:p.Glu923Asp
ENST00000368474.9:c.3654A>T MANE Select	ENSP00000357459.4:p.Glu1218Asp
ENST00000492630.2:n.2447A>T
ENST00000529168.2:c.3576A>T	ENSP00000431794.2:p.Glu1192Asp
ENST00000647682.2:n.3639A>T
ENST00000648231.2:c.2769A>T	ENSP00000497555.1:p.Glu923Asp
ENST00000648311.1:c.2769A>T	ENSP00000498137.1:p.Glu923Asp
ENST00000648714.2:c.*1129A>T	ENSP00000497434.2:n.*1129A>T
ENST00000649021.1:n.4390A>T
ENST00000649022.2:c.2769A>T	ENSP00000496896.2:p.Glu923Asp
ENST00000649042.1:c.2769A>T	ENSP00000497790.1:p.Glu923Asp
ENST00000649408.2:c.*820A>T	ENSP00000497386.2:n.*820A>T
ENST00000649724.1:c.2769A>T	ENSP00000497932.1:p.Glu923Asp
ENST00000649749.1:c.2769A>T	ENSP00000497210.1:p.Glu923Asp
ENST00000679375.1:c.*1886A>T	ENSP00000505887.1:n.*1886A>T
ENST00000679465.1:n.4515A>T
ENST00000679805.1:n.4390A>T
ENST00000679899.1:c.2712A>T	ENSP00000505996.1:p.Glu904Asp
ENST00000680270.1:c.2769A>T	ENSP00000505532.1:p.Glu923Asp
ENST00000680305.1:c.3471A>T	ENSP00000506312.1:p.Glu1157Asp
ENST00000681056.1:c.2769A>T	ENSP00000506234.1:p.Glu923Asp
ENST00000681235.1:c.*3176A>T	ENSP00000506606.1:n.*3176A>T
ENST00000681429.1:n.3322A>T
ENST00000681683.1:c.2769A>T	ENSP00000506666.1:p.Glu923Asp
ENST00000681786.1:n.4515A>T
ENST00000681901.1:c.*3254A>T	ENSP00000504883.1:n.*3254A>T
ENST00000368471.7:c.2769A>T	ENSP00000357456.3:p.Glu923Asp
ENST00000368474.8:c.3654A>T	ENSP00000357459.4:p.Glu1218Asp
ENST00000492630.1:n.413A>T
ENST00000529168.1:c.3561A>T	ENSP00000431794.1:p.Glu1187Asp
NM_001025107.2:c.2769A>T	NP_001020278.1:p.Glu923Asp
NM_001111.4:c.3654A>T	NP_001102.2:p.Glu1218Asp
NM_001193495.1:c.2769A>T	NP_001180424.1:p.Glu923Asp
NM_015840.3:c.3576A>T	NP_056655.2:p.Glu1192Asp
NM_015841.3:c.3519A>T	NP_056656.2:p.Glu1173Asp
XM_006711109.1:c.3684A>T	XP_006711172.1:p.Glu1228Asp
XM_006711111.2:c.2769A>T	XP_006711174.1:p.Glu923Asp
XM_006711112.1:c.2769A>T	XP_006711175.1:p.Glu923Asp
XM_006711113.1:c.2769A>T	XP_006711176.1:p.Glu923Asp
XM_011509060.1:c.3783A>T	XP_011507362.1:p.Glu1261Asp
XM_011509061.1:c.3705A>T	XP_011507363.1:p.Glu1235Asp
XM_011509062.1:c.3672A>T	XP_011507364.1:p.Glu1224Asp
NM_001025107.3:c.2769A>T	NP_001020278.1:p.Glu923Asp
NM_001111.5:c.3654A>T MANE Select	NP_001102.3:p.Glu1218Asp
NM_001193495.2:c.2769A>T	NP_001180424.1:p.Glu923Asp
NM_001365045.1:c.3681A>T	NP_001351974.1:p.Glu1227Asp
NM_001365046.1:c.2769A>T	NP_001351975.1:p.Glu923Asp
NM_001365047.1:c.2769A>T	NP_001351976.1:p.Glu923Asp
NM_001365048.1:c.2769A>T	NP_001351977.1:p.Glu923Asp
NM_001365049.1:c.2691A>T	NP_001351978.1:p.Glu897Asp
NM_015840.4:c.3576A>T	NP_056655.3:p.Glu1192Asp
NM_015841.4:c.3519A>T	NP_056656.3:p.Glu1173Asp
XM_006711113.2:c.2769A>T	XP_006711176.1:p.Glu923Asp
XM_011509061.2:c.2691A>T	XP_011507363.2:p.Glu897Asp
XM_024449674.1:c.3783A>T	XP_024305442.1:p.Glu1261Asp