Canonical Allele Identifier: CA2480932968
Gene: ADAR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154589226_154589227delinsCG , CM000663.2:g.154589226_154589227delinsCG GRCh38
NC_000001.10:g.154561702_154561703delinsCG , CM000663.1:g.154561702_154561703delinsCG GRCh37
NC_000001.9:g.152828326_152828327delinsCG NCBI36
NG_011844.1:g.43735_43736delinsCG
NG_011844.2:g.47334_47335delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2656+142_2656+143delinsCG ENSP00000497790.2:n.2656+142_2656+143delinsCG
ENST00000649724.2:c.2792+142_2792+143delinsCG ENSP00000497932.2:n.2792+142_2792+143delinsCG
ENST00000680270.2:c.2645+142_2645+143delinsCG ENSP00000505532.2:n.2645+142_2645+143delinsCG
ENST00000681056.2:c.2414+142_2414+143delinsCG ENSP00000506234.2:n.2414+142_2414+143delinsCG
ENST00000368471.8:c.1877+142_1877+143delinsCG ENSP00000357456.3:n.1877+142_1877+143delinsCG
ENST00000368474.9:c.2762+142_2762+143delinsCG MANE Select ENSP00000357459.4:n.2762+142_2762+143delinsCG
ENST00000529168.2:c.2684+142_2684+143delinsCG ENSP00000431794.2:n.2684+142_2684+143delinsCG
ENST00000647682.2:n.2747+142_2747+143delinsCG
ENST00000648231.2:c.1877+142_1877+143delinsCG ENSP00000497555.1:n.1877+142_1877+143delinsCG
ENST00000648311.1:c.1877+142_1877+143delinsCG ENSP00000498137.1:n.1877+142_1877+143delinsCG
ENST00000648714.2:c.*237+142_*237+143delinsCG ENSP00000497434.2:n.*237+142_*237+143delinsCG
ENST00000649021.1:n.2798+142_2798+143delinsCG
ENST00000649022.2:c.1877+142_1877+143delinsCG ENSP00000496896.2:n.1877+142_1877+143delinsCG
ENST00000649042.1:c.1877+142_1877+143delinsCG ENSP00000497790.1:n.1877+142_1877+143delinsCG
ENST00000649408.2:c.2762+142_2762+143delinsCG ENSP00000497386.2:n.2762+142_2762+143delinsCG
ENST00000649724.1:c.1877+142_1877+143delinsCG ENSP00000497932.1:n.1877+142_1877+143delinsCG
ENST00000649749.1:c.1877+142_1877+143delinsCG ENSP00000497210.1:n.1877+142_1877+143delinsCG
ENST00000679375.1:c.*994+142_*994+143delinsCG ENSP00000505887.1:n.*994+142_*994+143delinsCG
ENST00000679465.1:n.3215+142_3215+143delinsCG
ENST00000679805.1:n.2798+142_2798+143delinsCG
ENST00000679899.1:c.1820+142_1820+143delinsCG ENSP00000505996.1:n.1820+142_1820+143delinsCG
ENST00000680270.1:c.1877+142_1877+143delinsCG ENSP00000505532.1:n.1877+142_1877+143delinsCG
ENST00000680305.1:c.2762+142_2762+143delinsCG ENSP00000506312.1:n.2762+142_2762+143delinsCG
ENST00000681056.1:c.1877+142_1877+143delinsCG ENSP00000506234.1:n.1877+142_1877+143delinsCG
ENST00000681235.1:c.*2284+142_*2284+143delinsCG ENSP00000506606.1:n.*2284+142_*2284+143delinsCG
ENST00000681429.1:n.2022+142_2022+143delinsCG
ENST00000681683.1:c.1877+142_1877+143delinsCG ENSP00000506666.1:n.1877+142_1877+143delinsCG
ENST00000681786.1:n.3215+142_3215+143delinsCG
ENST00000681901.1:c.*2362+142_*2362+143delinsCG ENSP00000504883.1:n.*2362+142_*2362+143delinsCG
ENST00000368471.7:c.1877+142_1877+143delinsCG ENSP00000357456.3:n.1877+142_1877+143delinsCG
ENST00000368474.8:c.2762+142_2762+143delinsCG ENSP00000357459.4:n.2762+142_2762+143delinsCG
ENST00000529168.1:c.2669+142_2669+143delinsCG ENSP00000431794.1:n.2669+142_2669+143delinsCG
NM_001025107.2:c.1877+142_1877+143delinsCG NP_001020278.1:n.1877+142_1877+143delinsCG
NM_001111.4:c.2762+142_2762+143delinsCG NP_001102.2:n.2762+142_2762+143delinsCG
NM_001193495.1:c.1877+142_1877+143delinsCG NP_001180424.1:n.1877+142_1877+143delinsCG
NM_015840.3:c.2684+142_2684+143delinsCG NP_056655.2:n.2684+142_2684+143delinsCG
NM_015841.3:c.2627+142_2627+143delinsCG NP_056656.2:n.2627+142_2627+143delinsCG
XM_006711109.1:c.2792+142_2792+143delinsCG XP_006711172.1:n.2792+142_2792+143delinsCG
XM_006711111.2:c.1877+142_1877+143delinsCG XP_006711174.1:n.1877+142_1877+143delinsCG
XM_006711112.1:c.1877+142_1877+143delinsCG XP_006711175.1:n.1877+142_1877+143delinsCG
XM_006711113.1:c.1877+142_1877+143delinsCG XP_006711176.1:n.1877+142_1877+143delinsCG
XM_011509060.1:c.2891+142_2891+143delinsCG XP_011507362.1:n.2891+142_2891+143delinsCG
XM_011509061.1:c.2813+142_2813+143delinsCG XP_011507363.1:n.2813+142_2813+143delinsCG
XM_011509062.1:c.2780+142_2780+143delinsCG XP_011507364.1:n.2780+142_2780+143delinsCG
NM_001025107.3:c.1877+142_1877+143delinsCG NP_001020278.1:n.1877+142_1877+143delinsCG
NM_001111.5:c.2762+142_2762+143delinsCG MANE Select NP_001102.3:n.2762+142_2762+143delinsCG
NM_001193495.2:c.1877+142_1877+143delinsCG NP_001180424.1:n.1877+142_1877+143delinsCG
NM_001365045.1:c.2789+142_2789+143delinsCG NP_001351974.1:n.2789+142_2789+143delinsCG
NM_001365046.1:c.1877+142_1877+143delinsCG NP_001351975.1:n.1877+142_1877+143delinsCG
NM_001365047.1:c.1877+142_1877+143delinsCG NP_001351976.1:n.1877+142_1877+143delinsCG
NM_001365048.1:c.1877+142_1877+143delinsCG NP_001351977.1:n.1877+142_1877+143delinsCG
NM_001365049.1:c.1799+142_1799+143delinsCG NP_001351978.1:n.1799+142_1799+143delinsCG
NM_015840.4:c.2684+142_2684+143delinsCG NP_056655.3:n.2684+142_2684+143delinsCG
NM_015841.4:c.2627+142_2627+143delinsCG NP_056656.3:n.2627+142_2627+143delinsCG
XM_006711113.2:c.1877+142_1877+143delinsCG XP_006711176.1:n.1877+142_1877+143delinsCG
XM_011509061.2:c.1799+142_1799+143delinsCG XP_011507363.2:n.1799+142_1799+143delinsCG
XM_024449674.1:c.2891+142_2891+143delinsCG XP_024305442.1:n.2891+142_2891+143delinsCG
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