Canonical Allele Identifier: CA889612807
Gene: ADAR HGNC NCBI

Linked Data

dbSNP Id: rs1451717993

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154589703_154589704del , CM000663.2:g.154589703_154589704del GRCh38
NC_000001.10:g.154562179_154562180del , CM000663.1:g.154562179_154562180del GRCh37
NC_000001.9:g.152828803_152828804del NCBI36
NG_011844.1:g.43261_43262del
NG_011844.2:g.46860_46861del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2562+56_2562+57del ENSP00000497790.2:n.2562+56_2562+57del
ENST00000649724.2:c.2698+56_2698+57del ENSP00000497932.2:n.2698+56_2698+57del
ENST00000680270.2:c.2551+56_2551+57del ENSP00000505532.2:n.2551+56_2551+57del
ENST00000681056.2:c.2320+56_2320+57del ENSP00000506234.2:n.2320+56_2320+57del
ENST00000368471.8:c.1783+56_1783+57del ENSP00000357456.3:n.1783+56_1783+57del
ENST00000368474.9:c.2668+56_2668+57del MANE Select ENSP00000357459.4:n.2668+56_2668+57del
ENST00000529168.2:c.2590+56_2590+57del ENSP00000431794.2:n.2590+56_2590+57del
ENST00000647682.2:n.2653+56_2653+57del
ENST00000648231.2:c.1783+56_1783+57del ENSP00000497555.1:n.1783+56_1783+57del
ENST00000648311.1:c.1783+56_1783+57del ENSP00000498137.1:n.1783+56_1783+57del
ENST00000648714.2:c.*143+56_*143+57del ENSP00000497434.2:n.*143+56_*143+57del
ENST00000649021.1:n.2704+56_2704+57del
ENST00000649022.2:c.1783+56_1783+57del ENSP00000496896.2:n.1783+56_1783+57del
ENST00000649042.1:c.1783+56_1783+57del ENSP00000497790.1:n.1783+56_1783+57del
ENST00000649408.2:c.2668+56_2668+57del ENSP00000497386.2:n.2668+56_2668+57del
ENST00000649724.1:c.1783+56_1783+57del ENSP00000497932.1:n.1783+56_1783+57del
ENST00000649749.1:c.1783+56_1783+57del ENSP00000497210.1:n.1783+56_1783+57del
ENST00000679375.1:c.*900+56_*900+57del ENSP00000505887.1:n.*900+56_*900+57del
ENST00000679465.1:n.3121+56_3121+57del
ENST00000679805.1:n.2704+56_2704+57del
ENST00000679899.1:c.1726+56_1726+57del ENSP00000505996.1:n.1726+56_1726+57del
ENST00000680270.1:c.1783+56_1783+57del ENSP00000505532.1:n.1783+56_1783+57del
ENST00000680305.1:c.2668+56_2668+57del ENSP00000506312.1:n.2668+56_2668+57del
ENST00000681056.1:c.1783+56_1783+57del ENSP00000506234.1:n.1783+56_1783+57del
ENST00000681235.1:c.*2190+56_*2190+57del ENSP00000506606.1:n.*2190+56_*2190+57del
ENST00000681429.1:n.1928+56_1928+57del
ENST00000681683.1:c.1783+56_1783+57del ENSP00000506666.1:n.1783+56_1783+57del
ENST00000681786.1:n.3121+56_3121+57del
ENST00000681901.1:c.*2268+56_*2268+57del ENSP00000504883.1:n.*2268+56_*2268+57del
ENST00000368471.7:c.1783+56_1783+57del ENSP00000357456.3:n.1783+56_1783+57del
ENST00000368474.8:c.2668+56_2668+57del ENSP00000357459.4:n.2668+56_2668+57del
ENST00000529168.1:c.2575+56_2575+57del ENSP00000431794.1:n.2575+56_2575+57del
NM_001025107.2:c.1783+56_1783+57del NP_001020278.1:n.1783+56_1783+57del
NM_001111.4:c.2668+56_2668+57del NP_001102.2:n.2668+56_2668+57del
NM_001193495.1:c.1783+56_1783+57del NP_001180424.1:n.1783+56_1783+57del
NM_015840.3:c.2590+56_2590+57del NP_056655.2:n.2590+56_2590+57del
NM_015841.3:c.2533+56_2533+57del NP_056656.2:n.2533+56_2533+57del
XM_006711109.1:c.2698+56_2698+57del XP_006711172.1:n.2698+56_2698+57del
XM_006711111.2:c.1783+56_1783+57del XP_006711174.1:n.1783+56_1783+57del
XM_006711112.1:c.1783+56_1783+57del XP_006711175.1:n.1783+56_1783+57del
XM_006711113.1:c.1783+56_1783+57del XP_006711176.1:n.1783+56_1783+57del
XM_011509060.1:c.2797+56_2797+57del XP_011507362.1:n.2797+56_2797+57del
XM_011509061.1:c.2719+56_2719+57del XP_011507363.1:n.2719+56_2719+57del
XM_011509062.1:c.2686+56_2686+57del XP_011507364.1:n.2686+56_2686+57del
NM_001025107.3:c.1783+56_1783+57del NP_001020278.1:n.1783+56_1783+57del
NM_001111.5:c.2668+56_2668+57del MANE Select NP_001102.3:n.2668+56_2668+57del
NM_001193495.2:c.1783+56_1783+57del NP_001180424.1:n.1783+56_1783+57del
NM_001365045.1:c.2695+56_2695+57del NP_001351974.1:n.2695+56_2695+57del
NM_001365046.1:c.1783+56_1783+57del NP_001351975.1:n.1783+56_1783+57del
NM_001365047.1:c.1783+56_1783+57del NP_001351976.1:n.1783+56_1783+57del
NM_001365048.1:c.1783+56_1783+57del NP_001351977.1:n.1783+56_1783+57del
NM_001365049.1:c.1705+56_1705+57del NP_001351978.1:n.1705+56_1705+57del
NM_015840.4:c.2590+56_2590+57del NP_056655.3:n.2590+56_2590+57del
NM_015841.4:c.2533+56_2533+57del NP_056656.3:n.2533+56_2533+57del
XM_006711113.2:c.1783+56_1783+57del XP_006711176.1:n.1783+56_1783+57del
XM_011509061.2:c.1705+56_1705+57del XP_011507363.2:n.1705+56_1705+57del
XM_024449674.1:c.2797+56_2797+57del XP_024305442.1:n.2797+56_2797+57del