Canonical Allele Identifier: CA2586967366
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154601255_154601259del , CM000663.2:g.154601255_154601259del GRCh38
NC_000001.10:g.154573731_154573735del , CM000663.1:g.154573731_154573735del GRCh37
NC_000001.9:g.152840355_152840359del NCBI36
NG_011844.1:g.31706_31710del
NG_011844.2:g.35305_35309del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.1280_1284del ENSP00000497790.2:n.1280_1284del
ENST00000649724.2:c.1416_1420del ENSP00000497932.2:p.Asp472GlufsTer2
ENST00000680270.2:c.1269_1273del ENSP00000505532.2:p.Asp423GlufsTer2
ENST00000681056.2:c.1038_1042del ENSP00000506234.2:p.Asp346GlufsTer2
ENST00000368471.8:c.501_505del ENSP00000357456.3:p.Asp167GlufsTer2
ENST00000368474.9:c.1386_1390del MANE Select ENSP00000357459.4:p.Asp462GlufsTer2
ENST00000529168.2:c.1386_1390del ENSP00000431794.2:p.Asp462GlufsTer2
ENST00000647682.2:n.1116_1120del
ENST00000648231.2:c.501_505del ENSP00000497555.1:p.Asp167GlufsTer2
ENST00000648311.1:c.501_505del ENSP00000498137.1:p.Asp167GlufsTer2
ENST00000648714.2:c.1386_1390del ENSP00000497434.2:p.Asp462GlufsTer2
ENST00000648871.1:c.501_505del ENSP00000497793.1:p.Asp167GlufsTer2
ENST00000649021.1:n.1422_1426del
ENST00000649022.2:c.501_505del ENSP00000496896.2:p.Asp167GlufsTer2
ENST00000649042.1:c.501_505del ENSP00000497790.1:p.Asp167GlufsTer2
ENST00000649408.2:c.1386_1390del ENSP00000497386.2:p.Asp462GlufsTer2
ENST00000649724.1:c.501_505del ENSP00000497932.1:p.Asp167GlufsTer2
ENST00000649749.1:c.501_505del ENSP00000497210.1:p.Asp167GlufsTer2
ENST00000679375.1:c.501_505del ENSP00000505887.1:p.Asp167GlufsTer2
ENST00000679465.1:n.1584_1588del
ENST00000679805.1:n.1422_1426del
ENST00000679899.1:c.501_505del ENSP00000505996.1:p.Asp167GlufsTer2
ENST00000680270.1:c.501_505del ENSP00000505532.1:p.Asp167GlufsTer2
ENST00000680305.1:c.1386_1390del ENSP00000506312.1:p.Asp462GlufsTer2
ENST00000680472.1:n.1425_1429del
ENST00000681056.1:c.501_505del ENSP00000506234.1:p.Asp167GlufsTer2
ENST00000681235.1:c.*986_*990del ENSP00000506606.1:n.*986_*990del
ENST00000681683.1:c.501_505del ENSP00000506666.1:p.Asp167GlufsTer2
ENST00000681786.1:n.1584_1588del
ENST00000681901.1:c.*986_*990del ENSP00000504883.1:n.*986_*990del
ENST00000368471.7:c.501_505del ENSP00000357456.3:p.Asp167GlufsTer2
ENST00000368474.8:c.1386_1390del ENSP00000357459.4:p.Asp462GlufsTer2
ENST00000463920.5:n.1268_1272del
ENST00000529168.1:c.1371_1375del ENSP00000431794.1:p.Asp457GlufsTer2
NM_001025107.2:c.501_505del NP_001020278.1:p.Asp167GlufsTer2
NM_001111.4:c.1386_1390del NP_001102.2:p.Asp462GlufsTer2
NM_001193495.1:c.501_505del NP_001180424.1:p.Asp167GlufsTer2
NM_015840.3:c.1386_1390del NP_056655.2:p.Asp462GlufsTer2
NM_015841.3:c.1386_1390del NP_056656.2:p.Asp462GlufsTer2
XM_006711109.1:c.1416_1420del XP_006711172.1:p.Asp472GlufsTer2
XM_006711111.2:c.501_505del XP_006711174.1:p.Asp167GlufsTer2
XM_006711112.1:c.501_505del XP_006711175.1:p.Asp167GlufsTer2
XM_006711113.1:c.501_505del XP_006711176.1:p.Asp167GlufsTer2
XM_011509060.1:c.1515_1519del XP_011507362.1:p.Asp505GlufsTer2
XM_011509061.1:c.1515_1519del XP_011507363.1:p.Asp505GlufsTer2
XM_011509062.1:c.1404_1408del XP_011507364.1:p.Asp468GlufsTer2
NM_001025107.3:c.501_505del NP_001020278.1:p.Asp167GlufsTer2
NM_001111.5:c.1386_1390del MANE Select NP_001102.3:p.Asp462GlufsTer2
NM_001193495.2:c.501_505del NP_001180424.1:p.Asp167GlufsTer2
NM_001365045.1:c.1413_1417del NP_001351974.1:p.Asp471GlufsTer2
NM_001365046.1:c.501_505del NP_001351975.1:p.Asp167GlufsTer2
NM_001365047.1:c.501_505del NP_001351976.1:p.Asp167GlufsTer2
NM_001365048.1:c.501_505del NP_001351977.1:p.Asp167GlufsTer2
NM_001365049.1:c.501_505del NP_001351978.1:p.Asp167GlufsTer2
NM_015840.4:c.1386_1390del NP_056655.3:p.Asp462GlufsTer2
NM_015841.4:c.1386_1390del NP_056656.3:p.Asp462GlufsTer2
XM_006711113.2:c.501_505del XP_006711176.1:p.Asp167GlufsTer2
XM_011509061.2:c.501_505del XP_011507363.2:p.Asp167GlufsTer2
XM_024449674.1:c.1515_1519del XP_024305442.1:p.Asp505GlufsTer2