Canonical Allele Identifier: CA2480933215
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154589811T= , CM000663.2:g.154589811T= GRCh38
NC_000001.10:g.154562287T= , CM000663.1:g.154562287T= GRCh37
NC_000001.9:g.152828911T= NCBI36
NG_011844.1:g.43151A=
NG_011844.2:g.46750A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2508A= ENSP00000497790.2:n.2508A=
ENST00000649724.2:c.2644A= ENSP00000497932.2:p.Ile882=
ENST00000680270.2:c.2497A= ENSP00000505532.2:p.Ile833=
ENST00000681056.2:c.2266A= ENSP00000506234.2:p.Ile756=
ENST00000368471.8:c.1729A= ENSP00000357456.3:p.Ile577=
ENST00000368474.9:c.2614A= MANE Select ENSP00000357459.4:p.Ile872=
ENST00000529168.2:c.2536A= ENSP00000431794.2:p.Ile846=
ENST00000647682.2:n.2599A=
ENST00000648231.2:c.1729A= ENSP00000497555.1:p.Ile577=
ENST00000648311.1:c.1729A= ENSP00000498137.1:p.Ile577=
ENST00000648714.2:c.*89A= ENSP00000497434.2:n.*89A=
ENST00000649021.1:n.2650A=
ENST00000649022.2:c.1729A= ENSP00000496896.2:p.Ile577=
ENST00000649042.1:c.1729A= ENSP00000497790.1:p.Ile577=
ENST00000649408.2:c.2614A= ENSP00000497386.2:p.Ile872=
ENST00000649724.1:c.1729A= ENSP00000497932.1:p.Ile577=
ENST00000649749.1:c.1729A= ENSP00000497210.1:p.Ile577=
ENST00000679375.1:c.*846A= ENSP00000505887.1:n.*846A=
ENST00000679465.1:n.3067A=
ENST00000679805.1:n.2650A=
ENST00000679899.1:c.1672A= ENSP00000505996.1:p.Ile558=
ENST00000680270.1:c.1729A= ENSP00000505532.1:p.Ile577=
ENST00000680305.1:c.2614A= ENSP00000506312.1:p.Ile872=
ENST00000681056.1:c.1729A= ENSP00000506234.1:p.Ile577=
ENST00000681235.1:c.*2136A= ENSP00000506606.1:n.*2136A=
ENST00000681429.1:n.1874A=
ENST00000681683.1:c.1729A= ENSP00000506666.1:p.Ile577=
ENST00000681786.1:n.3067A=
ENST00000681901.1:c.*2214A= ENSP00000504883.1:n.*2214A=
ENST00000368471.7:c.1729A= ENSP00000357456.3:p.Ile577=
ENST00000368474.8:c.2614A= ENSP00000357459.4:p.Ile872=
ENST00000529168.1:c.2521A= ENSP00000431794.1:p.Ile841=
NM_001025107.2:c.1729A= NP_001020278.1:p.Ile577=
NM_001111.4:c.2614A= NP_001102.2:p.Ile872=
NM_001193495.1:c.1729A= NP_001180424.1:p.Ile577=
NM_015840.3:c.2536A= NP_056655.2:p.Ile846=
NM_015841.3:c.2479A= NP_056656.2:p.Ile827=
XM_006711109.1:c.2644A= XP_006711172.1:p.Ile882=
XM_006711111.2:c.1729A= XP_006711174.1:p.Ile577=
XM_006711112.1:c.1729A= XP_006711175.1:p.Ile577=
XM_006711113.1:c.1729A= XP_006711176.1:p.Ile577=
XM_011509060.1:c.2743A= XP_011507362.1:p.Ile915=
XM_011509061.1:c.2665A= XP_011507363.1:p.Ile889=
XM_011509062.1:c.2632A= XP_011507364.1:p.Ile878=
NM_001025107.3:c.1729A= NP_001020278.1:p.Ile577=
NM_001111.5:c.2614A= MANE Select NP_001102.3:p.Ile872=
NM_001193495.2:c.1729A= NP_001180424.1:p.Ile577=
NM_001365045.1:c.2641A= NP_001351974.1:p.Ile881=
NM_001365046.1:c.1729A= NP_001351975.1:p.Ile577=
NM_001365047.1:c.1729A= NP_001351976.1:p.Ile577=
NM_001365048.1:c.1729A= NP_001351977.1:p.Ile577=
NM_001365049.1:c.1651A= NP_001351978.1:p.Ile551=
NM_015840.4:c.2536A= NP_056655.3:p.Ile846=
NM_015841.4:c.2479A= NP_056656.3:p.Ile827=
XM_006711113.2:c.1729A= XP_006711176.1:p.Ile577=
XM_011509061.2:c.1651A= XP_011507363.2:p.Ile551=
XM_024449674.1:c.2743A= XP_024305442.1:p.Ile915=