Canonical Allele Identifier: CA2480931185
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154584841G= , CM000663.2:g.154584841G= GRCh38
NC_000001.10:g.154557317G= , CM000663.1:g.154557317G= GRCh37
NC_000001.9:g.152823941G= NCBI36
NG_011844.1:g.48121C=
NG_011844.2:g.51720C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.3540C= ENSP00000497790.2:n.3540C=
ENST00000649724.2:c.3676C= ENSP00000497932.2:p.Gln1226=
ENST00000680270.2:c.3529C= ENSP00000505532.2:p.Gln1177=
ENST00000681056.2:c.3298C= ENSP00000506234.2:p.Gln1100=
ENST00000368471.8:c.2761C= ENSP00000357456.3:p.Gln921=
ENST00000368474.9:c.3646C= MANE Select ENSP00000357459.4:p.Gln1216=
ENST00000492630.2:n.2439C=
ENST00000529168.2:c.3568C= ENSP00000431794.2:p.Gln1190=
ENST00000647682.2:n.3631C=
ENST00000648231.2:c.2761C= ENSP00000497555.1:p.Gln921=
ENST00000648311.1:c.2761C= ENSP00000498137.1:p.Gln921=
ENST00000648714.2:c.*1121C= ENSP00000497434.2:n.*1121C=
ENST00000649021.1:n.4382C=
ENST00000649022.2:c.2761C= ENSP00000496896.2:p.Gln921=
ENST00000649042.1:c.2761C= ENSP00000497790.1:p.Gln921=
ENST00000649408.2:c.*812C= ENSP00000497386.2:n.*812C=
ENST00000649724.1:c.2761C= ENSP00000497932.1:p.Gln921=
ENST00000649749.1:c.2761C= ENSP00000497210.1:p.Gln921=
ENST00000679375.1:c.*1878C= ENSP00000505887.1:n.*1878C=
ENST00000679465.1:n.4507C=
ENST00000679805.1:n.4382C=
ENST00000679899.1:c.2704C= ENSP00000505996.1:p.Gln902=
ENST00000680270.1:c.2761C= ENSP00000505532.1:p.Gln921=
ENST00000680305.1:c.3463C= ENSP00000506312.1:p.Gln1155=
ENST00000681056.1:c.2761C= ENSP00000506234.1:p.Gln921=
ENST00000681235.1:c.*3168C= ENSP00000506606.1:n.*3168C=
ENST00000681429.1:n.3314C=
ENST00000681683.1:c.2761C= ENSP00000506666.1:p.Gln921=
ENST00000681786.1:n.4507C=
ENST00000681901.1:c.*3246C= ENSP00000504883.1:n.*3246C=
ENST00000368471.7:c.2761C= ENSP00000357456.3:p.Gln921=
ENST00000368474.8:c.3646C= ENSP00000357459.4:p.Gln1216=
ENST00000492630.1:n.405C=
ENST00000529168.1:c.3553C= ENSP00000431794.1:p.Gln1185=
NM_001025107.2:c.2761C= NP_001020278.1:p.Gln921=
NM_001111.4:c.3646C= NP_001102.2:p.Gln1216=
NM_001193495.1:c.2761C= NP_001180424.1:p.Gln921=
NM_015840.3:c.3568C= NP_056655.2:p.Gln1190=
NM_015841.3:c.3511C= NP_056656.2:p.Gln1171=
XM_006711109.1:c.3676C= XP_006711172.1:p.Gln1226=
XM_006711111.2:c.2761C= XP_006711174.1:p.Gln921=
XM_006711112.1:c.2761C= XP_006711175.1:p.Gln921=
XM_006711113.1:c.2761C= XP_006711176.1:p.Gln921=
XM_011509060.1:c.3775C= XP_011507362.1:p.Gln1259=
XM_011509061.1:c.3697C= XP_011507363.1:p.Gln1233=
XM_011509062.1:c.3664C= XP_011507364.1:p.Gln1222=
NM_001025107.3:c.2761C= NP_001020278.1:p.Gln921=
NM_001111.5:c.3646C= MANE Select NP_001102.3:p.Gln1216=
NM_001193495.2:c.2761C= NP_001180424.1:p.Gln921=
NM_001365045.1:c.3673C= NP_001351974.1:p.Gln1225=
NM_001365046.1:c.2761C= NP_001351975.1:p.Gln921=
NM_001365047.1:c.2761C= NP_001351976.1:p.Gln921=
NM_001365048.1:c.2761C= NP_001351977.1:p.Gln921=
NM_001365049.1:c.2683C= NP_001351978.1:p.Gln895=
NM_015840.4:c.3568C= NP_056655.3:p.Gln1190=
NM_015841.4:c.3511C= NP_056656.3:p.Gln1171=
XM_006711113.2:c.2761C= XP_006711176.1:p.Gln921=
XM_011509061.2:c.2683C= XP_011507363.2:p.Gln895=
XM_024449674.1:c.3775C= XP_024305442.1:p.Gln1259=