Canonical Allele Identifier: CA2841902768
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154588187dup , CM000663.2:g.154588187dup GRCh38
NC_000001.10:g.154560663dup , CM000663.1:g.154560663dup GRCh37
NC_000001.9:g.152827287dup NCBI36
NG_011844.1:g.44777dup
NG_011844.2:g.48376dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2853dup ENSP00000497790.2:n.2853dup
ENST00000649724.2:c.2989dup ENSP00000497932.2:p.Arg997ProfsTer?
ENST00000680270.2:c.2842dup ENSP00000505532.2:p.Arg948ProfsTer?
ENST00000681056.2:c.2611dup ENSP00000506234.2:p.Arg871ProfsTer?
ENST00000368471.8:c.2074dup ENSP00000357456.3:p.Arg692ProfsTer?
ENST00000368474.9:c.2959dup MANE Select ENSP00000357459.4:p.Arg987ProfsTer?
ENST00000529168.2:c.2881dup ENSP00000431794.2:p.Arg961ProfsTer?
ENST00000647682.2:n.2944dup
ENST00000648231.2:c.2074dup ENSP00000497555.1:p.Arg692ProfsTer?
ENST00000648311.1:c.2074dup ENSP00000498137.1:p.Arg692ProfsTer?
ENST00000648714.2:c.*434dup ENSP00000497434.2:n.*434dup
ENST00000649021.1:n.3287dup
ENST00000649022.2:c.2074dup ENSP00000496896.2:p.Arg692ProfsTer?
ENST00000649042.1:c.2074dup ENSP00000497790.1:p.Arg692ProfsTer?
ENST00000649408.2:c.2959dup ENSP00000497386.2:p.Arg987ProfsTer?
ENST00000649724.1:c.2074dup ENSP00000497932.1:p.Arg692ProfsTer?
ENST00000649749.1:c.2074dup ENSP00000497210.1:p.Arg692ProfsTer?
ENST00000679375.1:c.*1191dup ENSP00000505887.1:n.*1191dup
ENST00000679465.1:n.3412dup
ENST00000679805.1:n.3287dup
ENST00000679899.1:c.2017dup ENSP00000505996.1:p.Arg673ProfsTer?
ENST00000680270.1:c.2074dup ENSP00000505532.1:p.Arg692ProfsTer?
ENST00000680305.1:c.2959dup ENSP00000506312.1:p.Arg987ProfsTer?
ENST00000681056.1:c.2074dup ENSP00000506234.1:p.Arg692ProfsTer?
ENST00000681235.1:c.*2481dup ENSP00000506606.1:n.*2481dup
ENST00000681429.1:n.2219dup
ENST00000681683.1:c.2074dup ENSP00000506666.1:p.Arg692ProfsTer?
ENST00000681786.1:n.3412dup
ENST00000681901.1:c.*2559dup ENSP00000504883.1:n.*2559dup
ENST00000368471.7:c.2074dup ENSP00000357456.3:p.Arg692ProfsTer?
ENST00000368474.8:c.2959dup ENSP00000357459.4:p.Arg987ProfsTer?
ENST00000529168.1:c.2866dup ENSP00000431794.1:p.Arg956ProfsTer?
ENST00000530954.1:n.96dup
ENST00000534279.1:n.418dup
NM_001025107.2:c.2074dup NP_001020278.1:p.Arg692ProfsTer?
NM_001111.4:c.2959dup NP_001102.2:p.Arg987ProfsTer?
NM_001193495.1:c.2074dup NP_001180424.1:p.Arg692ProfsTer?
NM_015840.3:c.2881dup NP_056655.2:p.Arg961ProfsTer?
NM_015841.3:c.2824dup NP_056656.2:p.Arg942ProfsTer?
XM_006711109.1:c.2989dup XP_006711172.1:p.Arg997ProfsTer?
XM_006711111.2:c.2074dup XP_006711174.1:p.Arg692ProfsTer?
XM_006711112.1:c.2074dup XP_006711175.1:p.Arg692ProfsTer?
XM_006711113.1:c.2074dup XP_006711176.1:p.Arg692ProfsTer?
XM_011509060.1:c.3088dup XP_011507362.1:p.Arg1030ProfsTer?
XM_011509061.1:c.3010dup XP_011507363.1:p.Arg1004ProfsTer?
XM_011509062.1:c.2977dup XP_011507364.1:p.Arg993ProfsTer?
NM_001025107.3:c.2074dup NP_001020278.1:p.Arg692ProfsTer?
NM_001111.5:c.2959dup MANE Select NP_001102.3:p.Arg987ProfsTer?
NM_001193495.2:c.2074dup NP_001180424.1:p.Arg692ProfsTer?
NM_001365045.1:c.2986dup NP_001351974.1:p.Arg996ProfsTer?
NM_001365046.1:c.2074dup NP_001351975.1:p.Arg692ProfsTer?
NM_001365047.1:c.2074dup NP_001351976.1:p.Arg692ProfsTer?
NM_001365048.1:c.2074dup NP_001351977.1:p.Arg692ProfsTer?
NM_001365049.1:c.1996dup NP_001351978.1:p.Arg666ProfsTer?
NM_015840.4:c.2881dup NP_056655.3:p.Arg961ProfsTer?
NM_015841.4:c.2824dup NP_056656.3:p.Arg942ProfsTer?
XM_006711113.2:c.2074dup XP_006711176.1:p.Arg692ProfsTer?
XM_011509061.2:c.1996dup XP_011507363.2:p.Arg666ProfsTer?
XM_024449674.1:c.3088dup XP_024305442.1:p.Arg1030ProfsTer?