Canonical Allele Identifier: CA342636529
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 2954166
ClinVar RCV Id: RCV003813389

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154589373T>C , CM000663.2:g.154589373T>C GRCh38
NC_000001.10:g.154561849T>C , CM000663.1:g.154561849T>C GRCh37
NC_000001.9:g.152828473T>C NCBI36
NG_011844.1:g.43589A>G
NG_011844.2:g.47188A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2652A>G ENSP00000497790.2:n.2652A>G
ENST00000649724.2:c.2788A>G ENSP00000497932.2:p.Ile930Val
ENST00000680270.2:c.2641A>G ENSP00000505532.2:p.Ile881Val
ENST00000681056.2:c.2410A>G ENSP00000506234.2:p.Ile804Val
ENST00000368471.8:c.1873A>G ENSP00000357456.3:p.Ile625Val
ENST00000368474.9:c.2758A>G MANE Select ENSP00000357459.4:p.Ile920Val
ENST00000529168.2:c.2680A>G ENSP00000431794.2:p.Ile894Val
ENST00000647682.2:n.2743A>G
ENST00000648231.2:c.1873A>G ENSP00000497555.1:p.Ile625Val
ENST00000648311.1:c.1873A>G ENSP00000498137.1:p.Ile625Val
ENST00000648714.2:c.*233A>G ENSP00000497434.2:n.*233A>G
ENST00000649021.1:n.2794A>G
ENST00000649022.2:c.1873A>G ENSP00000496896.2:p.Ile625Val
ENST00000649042.1:c.1873A>G ENSP00000497790.1:p.Ile625Val
ENST00000649408.2:c.2758A>G ENSP00000497386.2:p.Ile920Val
ENST00000649724.1:c.1873A>G ENSP00000497932.1:p.Ile625Val
ENST00000649749.1:c.1873A>G ENSP00000497210.1:p.Ile625Val
ENST00000679375.1:c.*990A>G ENSP00000505887.1:n.*990A>G
ENST00000679465.1:n.3211A>G
ENST00000679805.1:n.2794A>G
ENST00000679899.1:c.1816A>G ENSP00000505996.1:p.Ile606Val
ENST00000680270.1:c.1873A>G ENSP00000505532.1:p.Ile625Val
ENST00000680305.1:c.2758A>G ENSP00000506312.1:p.Ile920Val
ENST00000681056.1:c.1873A>G ENSP00000506234.1:p.Ile625Val
ENST00000681235.1:c.*2280A>G ENSP00000506606.1:n.*2280A>G
ENST00000681429.1:n.2018A>G
ENST00000681683.1:c.1873A>G ENSP00000506666.1:p.Ile625Val
ENST00000681786.1:n.3211A>G
ENST00000681901.1:c.*2358A>G ENSP00000504883.1:n.*2358A>G
ENST00000368471.7:c.1873A>G ENSP00000357456.3:p.Ile625Val
ENST00000368474.8:c.2758A>G ENSP00000357459.4:p.Ile920Val
ENST00000529168.1:c.2665A>G ENSP00000431794.1:p.Ile889Val
NM_001025107.2:c.1873A>G NP_001020278.1:p.Ile625Val
NM_001111.4:c.2758A>G NP_001102.2:p.Ile920Val
NM_001193495.1:c.1873A>G NP_001180424.1:p.Ile625Val
NM_015840.3:c.2680A>G NP_056655.2:p.Ile894Val
NM_015841.3:c.2623A>G NP_056656.2:p.Ile875Val
XM_006711109.1:c.2788A>G XP_006711172.1:p.Ile930Val
XM_006711111.2:c.1873A>G XP_006711174.1:p.Ile625Val
XM_006711112.1:c.1873A>G XP_006711175.1:p.Ile625Val
XM_006711113.1:c.1873A>G XP_006711176.1:p.Ile625Val
XM_011509060.1:c.2887A>G XP_011507362.1:p.Ile963Val
XM_011509061.1:c.2809A>G XP_011507363.1:p.Ile937Val
XM_011509062.1:c.2776A>G XP_011507364.1:p.Ile926Val
NM_001025107.3:c.1873A>G NP_001020278.1:p.Ile625Val
NM_001111.5:c.2758A>G MANE Select NP_001102.3:p.Ile920Val
NM_001193495.2:c.1873A>G NP_001180424.1:p.Ile625Val
NM_001365045.1:c.2785A>G NP_001351974.1:p.Ile929Val
NM_001365046.1:c.1873A>G NP_001351975.1:p.Ile625Val
NM_001365047.1:c.1873A>G NP_001351976.1:p.Ile625Val
NM_001365048.1:c.1873A>G NP_001351977.1:p.Ile625Val
NM_001365049.1:c.1795A>G NP_001351978.1:p.Ile599Val
NM_015840.4:c.2680A>G NP_056655.3:p.Ile894Val
NM_015841.4:c.2623A>G NP_056656.3:p.Ile875Val
XM_006711113.2:c.1873A>G XP_006711176.1:p.Ile625Val
XM_011509061.2:c.1795A>G XP_011507363.2:p.Ile599Val
XM_024449674.1:c.2887A>G XP_024305442.1:p.Ile963Val