Canonical Allele Identifier: CA2480938608
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154602322C= , CM000663.2:g.154602322C= GRCh38
NC_000001.10:g.154574798C= , CM000663.1:g.154574798C= GRCh37
NC_000001.9:g.152841422C= NCBI36
NG_011844.1:g.30640G=
NG_011844.2:g.34239G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.287+63G= ENSP00000497790.2:n.287+63G=
ENST00000649724.2:c.350G= ENSP00000497932.2:p.Gly117=
ENST00000680270.2:c.350G= ENSP00000505532.2:p.Gly117=
ENST00000681056.2:c.46-74G= ENSP00000506234.2:n.46-74G=
ENST00000368471.8:c.-566G= ENSP00000357456.3:n.-566G=
ENST00000368474.9:c.320G= MANE Select ENSP00000357459.4:p.Gly107=
ENST00000471068.2:n.390+63G=
ENST00000526905.2:n.257+63G=
ENST00000529168.2:c.320G= ENSP00000431794.2:p.Gly107=
ENST00000647682.2:n.124-74G=
ENST00000648231.2:c.-566G= ENSP00000497555.1:n.-566G=
ENST00000648311.1:c.-566G= ENSP00000498137.1:n.-566G=
ENST00000648714.2:c.320G= ENSP00000497434.2:p.Gly107=
ENST00000648871.1:c.-492-74G= ENSP00000497793.1:n.-492-74G=
ENST00000649021.1:n.356G=
ENST00000649022.2:c.-566G= ENSP00000496896.2:n.-566G=
ENST00000649042.1:c.-493+63G= ENSP00000497790.1:n.-493+63G=
ENST00000649408.2:c.320G= ENSP00000497386.2:p.Gly107=
ENST00000649724.1:c.-566G= ENSP00000497932.1:n.-566G=
ENST00000649749.1:c.-566G= ENSP00000497210.1:n.-566G=
ENST00000679375.1:c.-492-74G= ENSP00000505887.1:n.-492-74G=
ENST00000679465.1:n.518G=
ENST00000679805.1:n.356G=
ENST00000679899.1:c.-566G= ENSP00000505996.1:n.-566G=
ENST00000680270.1:c.-419G= ENSP00000505532.1:n.-419G=
ENST00000680305.1:c.320G= ENSP00000506312.1:p.Gly107=
ENST00000680472.1:n.359G=
ENST00000681056.1:c.-492-74G= ENSP00000506234.1:n.-492-74G=
ENST00000681235.1:c.257+63G= ENSP00000506606.1:n.257+63G=
ENST00000681683.1:c.-493+63G= ENSP00000506666.1:n.-493+63G=
ENST00000681786.1:n.518G=
ENST00000681901.1:c.257+63G= ENSP00000504883.1:n.257+63G=
ENST00000368471.7:c.-566G= ENSP00000357456.3:n.-566G=
ENST00000368474.8:c.320G= ENSP00000357459.4:p.Gly107=
ENST00000463920.5:n.275+63G=
ENST00000471068.1:n.351G=
ENST00000494866.1:n.300+63G=
ENST00000526905.1:n.367G=
ENST00000529168.1:c.305G= ENSP00000431794.1:p.Gly102=
NM_001025107.2:c.-566G= NP_001020278.1:n.-566G=
NM_001111.4:c.320G= NP_001102.2:p.Gly107=
NM_001193495.1:c.-566G= NP_001180424.1:n.-566G=
NM_015840.3:c.320G= NP_056655.2:p.Gly107=
NM_015841.3:c.320G= NP_056656.2:p.Gly107=
XM_006711109.1:c.350G= XP_006711172.1:p.Gly117=
XM_006711111.2:c.-493+63G= XP_006711174.1:n.-493+63G=
XM_006711112.1:c.-493+63G= XP_006711175.1:n.-493+63G=
XM_006711113.1:c.-493+63G= XP_006711176.1:n.-493+63G=
XM_011509060.1:c.449G= XP_011507362.1:p.Gly150=
XM_011509061.1:c.449G= XP_011507363.1:p.Gly150=
XM_011509062.1:c.338G= XP_011507364.1:p.Gly113=
NM_001025107.3:c.-566G= NP_001020278.1:n.-566G=
NM_001111.5:c.320G= MANE Select NP_001102.3:p.Gly107=
NM_001193495.2:c.-566G= NP_001180424.1:n.-566G=
NM_001365045.1:c.347G= NP_001351974.1:p.Gly116=
NM_001365046.1:c.-493+63G= NP_001351975.1:n.-493+63G=
NM_001365047.1:c.-493+63G= NP_001351976.1:n.-493+63G=
NM_001365048.1:c.-566G= NP_001351977.1:n.-566G=
NM_001365049.1:c.-493+63G= NP_001351978.1:n.-493+63G=
NM_015840.4:c.320G= NP_056655.3:p.Gly107=
NM_015841.4:c.320G= NP_056656.3:p.Gly107=
XM_006711113.2:c.-493+63G= XP_006711176.1:n.-493+63G=
XM_011509061.2:c.-566G= XP_011507363.2:n.-566G=
XM_024449674.1:c.449G= XP_024305442.1:p.Gly150=