Canonical Allele Identifier: CA1142288301
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154588249C= , CM000663.2:g.154588249C= GRCh38
NC_000001.10:g.154560725C= , CM000663.1:g.154560725C= GRCh37
NC_000001.9:g.152827349C= NCBI36
NG_011844.1:g.44713G=
NG_011844.2:g.48312G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2789G= ENSP00000497790.2:n.2789G=
ENST00000649724.2:c.2925G= ENSP00000497932.2:p.Pro975=
ENST00000680270.2:c.2778G= ENSP00000505532.2:p.Pro926=
ENST00000681056.2:c.2547G= ENSP00000506234.2:p.Pro849=
ENST00000368471.8:c.2010G= ENSP00000357456.3:p.Pro670=
ENST00000368474.9:c.2895G= MANE Select ENSP00000357459.4:p.Pro965=
ENST00000529168.2:c.2817G= ENSP00000431794.2:p.Pro939=
ENST00000647682.2:n.2880G=
ENST00000648231.2:c.2010G= ENSP00000497555.1:p.Pro670=
ENST00000648311.1:c.2010G= ENSP00000498137.1:p.Pro670=
ENST00000648714.2:c.*370G= ENSP00000497434.2:n.*370G=
ENST00000649021.1:n.3223G=
ENST00000649022.2:c.2010G= ENSP00000496896.2:p.Pro670=
ENST00000649042.1:c.2010G= ENSP00000497790.1:p.Pro670=
ENST00000649408.2:c.2895G= ENSP00000497386.2:p.Pro965=
ENST00000649724.1:c.2010G= ENSP00000497932.1:p.Pro670=
ENST00000649749.1:c.2010G= ENSP00000497210.1:p.Pro670=
ENST00000679375.1:c.*1127G= ENSP00000505887.1:n.*1127G=
ENST00000679465.1:n.3348G=
ENST00000679805.1:n.3223G=
ENST00000679899.1:c.1953G= ENSP00000505996.1:p.Pro651=
ENST00000680270.1:c.2010G= ENSP00000505532.1:p.Pro670=
ENST00000680305.1:c.2895G= ENSP00000506312.1:p.Pro965=
ENST00000681056.1:c.2010G= ENSP00000506234.1:p.Pro670=
ENST00000681235.1:c.*2417G= ENSP00000506606.1:n.*2417G=
ENST00000681429.1:n.2155G=
ENST00000681683.1:c.2010G= ENSP00000506666.1:p.Pro670=
ENST00000681786.1:n.3348G=
ENST00000681901.1:c.*2495G= ENSP00000504883.1:n.*2495G=
ENST00000368471.7:c.2010G= ENSP00000357456.3:p.Pro670=
ENST00000368474.8:c.2895G= ENSP00000357459.4:p.Pro965=
ENST00000529168.1:c.2802G= ENSP00000431794.1:p.Pro934=
ENST00000530954.1:n.32G=
ENST00000534279.1:n.354G=
NM_001025107.2:c.2010G= NP_001020278.1:p.Pro670=
NM_001111.4:c.2895G= NP_001102.2:p.Pro965=
NM_001193495.1:c.2010G= NP_001180424.1:p.Pro670=
NM_015840.3:c.2817G= NP_056655.2:p.Pro939=
NM_015841.3:c.2760G= NP_056656.2:p.Pro920=
XM_006711109.1:c.2925G= XP_006711172.1:p.Pro975=
XM_006711111.2:c.2010G= XP_006711174.1:p.Pro670=
XM_006711112.1:c.2010G= XP_006711175.1:p.Pro670=
XM_006711113.1:c.2010G= XP_006711176.1:p.Pro670=
XM_011509060.1:c.3024G= XP_011507362.1:p.Pro1008=
XM_011509061.1:c.2946G= XP_011507363.1:p.Pro982=
XM_011509062.1:c.2913G= XP_011507364.1:p.Pro971=
NM_001025107.3:c.2010G= NP_001020278.1:p.Pro670=
NM_001111.5:c.2895G= MANE Select NP_001102.3:p.Pro965=
NM_001193495.2:c.2010G= NP_001180424.1:p.Pro670=
NM_001365045.1:c.2922G= NP_001351974.1:p.Pro974=
NM_001365046.1:c.2010G= NP_001351975.1:p.Pro670=
NM_001365047.1:c.2010G= NP_001351976.1:p.Pro670=
NM_001365048.1:c.2010G= NP_001351977.1:p.Pro670=
NM_001365049.1:c.1932G= NP_001351978.1:p.Pro644=
NM_015840.4:c.2817G= NP_056655.3:p.Pro939=
NM_015841.4:c.2760G= NP_056656.3:p.Pro920=
XM_006711113.2:c.2010G= XP_006711176.1:p.Pro670=
XM_011509061.2:c.1932G= XP_011507363.2:p.Pro644=
XM_024449674.1:c.3024G= XP_024305442.1:p.Pro1008=