Canonical Allele Identifier: CA2480933195
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154589749T= , CM000663.2:g.154589749T= GRCh38
NC_000001.10:g.154562225T= , CM000663.1:g.154562225T= GRCh37
NC_000001.9:g.152828849T= NCBI36
NG_011844.1:g.43213A=
NG_011844.2:g.46812A=

Transcript Alleles

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