Canonical Allele Identifier: CA342636812

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154562266C>T (hg19) ; chr1:g.154589790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589790C>T , CM000663.2:g.154589790C>T	GRCh38
NC_000001.10:g.154562266C>T , CM000663.1:g.154562266C>T	GRCh37
NC_000001.9:g.152828890C>T	NCBI36
NG_011844.1:g.43172G>A
NG_011844.2:g.46771G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2529G>A	ENSP00000497790.2:n.2529G>A
ENST00000649724.2:c.2665G>A	ENSP00000497932.2:p.Glu889Lys
ENST00000680270.2:c.2518G>A	ENSP00000505532.2:p.Glu840Lys
ENST00000681056.2:c.2287G>A	ENSP00000506234.2:p.Glu763Lys
ENST00000368471.8:c.1750G>A	ENSP00000357456.3:p.Glu584Lys
ENST00000368474.9:c.2635G>A MANE Select	ENSP00000357459.4:p.Glu879Lys
ENST00000529168.2:c.2557G>A	ENSP00000431794.2:p.Glu853Lys
ENST00000647682.2:n.2620G>A
ENST00000648231.2:c.1750G>A	ENSP00000497555.1:p.Glu584Lys
ENST00000648311.1:c.1750G>A	ENSP00000498137.1:p.Glu584Lys
ENST00000648714.2:c.*110G>A	ENSP00000497434.2:n.*110G>A
ENST00000649021.1:n.2671G>A
ENST00000649022.2:c.1750G>A	ENSP00000496896.2:p.Glu584Lys
ENST00000649042.1:c.1750G>A	ENSP00000497790.1:p.Glu584Lys
ENST00000649408.2:c.2635G>A	ENSP00000497386.2:p.Glu879Lys
ENST00000649724.1:c.1750G>A	ENSP00000497932.1:p.Glu584Lys
ENST00000649749.1:c.1750G>A	ENSP00000497210.1:p.Glu584Lys
ENST00000679375.1:c.*867G>A	ENSP00000505887.1:n.*867G>A
ENST00000679465.1:n.3088G>A
ENST00000679805.1:n.2671G>A
ENST00000679899.1:c.1693G>A	ENSP00000505996.1:p.Glu565Lys
ENST00000680270.1:c.1750G>A	ENSP00000505532.1:p.Glu584Lys
ENST00000680305.1:c.2635G>A	ENSP00000506312.1:p.Glu879Lys
ENST00000681056.1:c.1750G>A	ENSP00000506234.1:p.Glu584Lys
ENST00000681235.1:c.*2157G>A	ENSP00000506606.1:n.*2157G>A
ENST00000681429.1:n.1895G>A
ENST00000681683.1:c.1750G>A	ENSP00000506666.1:p.Glu584Lys
ENST00000681786.1:n.3088G>A
ENST00000681901.1:c.*2235G>A	ENSP00000504883.1:n.*2235G>A
ENST00000368471.7:c.1750G>A	ENSP00000357456.3:p.Glu584Lys
ENST00000368474.8:c.2635G>A	ENSP00000357459.4:p.Glu879Lys
ENST00000529168.1:c.2542G>A	ENSP00000431794.1:p.Glu848Lys
NM_001025107.2:c.1750G>A	NP_001020278.1:p.Glu584Lys
NM_001111.4:c.2635G>A	NP_001102.2:p.Glu879Lys
NM_001193495.1:c.1750G>A	NP_001180424.1:p.Glu584Lys
NM_015840.3:c.2557G>A	NP_056655.2:p.Glu853Lys
NM_015841.3:c.2500G>A	NP_056656.2:p.Glu834Lys
XM_006711109.1:c.2665G>A	XP_006711172.1:p.Glu889Lys
XM_006711111.2:c.1750G>A	XP_006711174.1:p.Glu584Lys
XM_006711112.1:c.1750G>A	XP_006711175.1:p.Glu584Lys
XM_006711113.1:c.1750G>A	XP_006711176.1:p.Glu584Lys
XM_011509060.1:c.2764G>A	XP_011507362.1:p.Glu922Lys
XM_011509061.1:c.2686G>A	XP_011507363.1:p.Glu896Lys
XM_011509062.1:c.2653G>A	XP_011507364.1:p.Glu885Lys
NM_001025107.3:c.1750G>A	NP_001020278.1:p.Glu584Lys
NM_001111.5:c.2635G>A MANE Select	NP_001102.3:p.Glu879Lys
NM_001193495.2:c.1750G>A	NP_001180424.1:p.Glu584Lys
NM_001365045.1:c.2662G>A	NP_001351974.1:p.Glu888Lys
NM_001365046.1:c.1750G>A	NP_001351975.1:p.Glu584Lys
NM_001365047.1:c.1750G>A	NP_001351976.1:p.Glu584Lys
NM_001365048.1:c.1750G>A	NP_001351977.1:p.Glu584Lys
NM_001365049.1:c.1672G>A	NP_001351978.1:p.Glu558Lys
NM_015840.4:c.2557G>A	NP_056655.3:p.Glu853Lys
NM_015841.4:c.2500G>A	NP_056656.3:p.Glu834Lys
XM_006711113.2:c.1750G>A	XP_006711176.1:p.Glu584Lys
XM_011509061.2:c.1672G>A	XP_011507363.2:p.Glu558Lys
XM_024449674.1:c.2764G>A	XP_024305442.1:p.Glu922Lys