Canonical Allele Identifier: CA342635926
Gene: ADAR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154588129C>A , CM000663.2:g.154588129C>A GRCh38
NC_000001.10:g.154560605C>A , CM000663.1:g.154560605C>A GRCh37
NC_000001.9:g.152827229C>A NCBI36
NG_011844.1:g.44833G>T
NG_011844.2:g.48432G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2909G>T ENSP00000497790.2:n.2909G>T
ENST00000649724.2:c.3045G>T ENSP00000497932.2:p.Glu1015Asp
ENST00000680270.2:c.2898G>T ENSP00000505532.2:p.Glu966Asp
ENST00000681056.2:c.2667G>T ENSP00000506234.2:p.Glu889Asp
ENST00000368471.8:c.2130G>T ENSP00000357456.3:p.Glu710Asp
ENST00000368474.9:c.3015G>T MANE Select ENSP00000357459.4:p.Glu1005Asp
ENST00000529168.2:c.2937G>T ENSP00000431794.2:p.Glu979Asp
ENST00000647682.2:n.3000G>T
ENST00000648231.2:c.2130G>T ENSP00000497555.1:p.Glu710Asp
ENST00000648311.1:c.2130G>T ENSP00000498137.1:p.Glu710Asp
ENST00000648714.2:c.*490G>T ENSP00000497434.2:n.*490G>T
ENST00000649021.1:n.3343G>T
ENST00000649022.2:c.2130G>T ENSP00000496896.2:p.Glu710Asp
ENST00000649042.1:c.2130G>T ENSP00000497790.1:p.Glu710Asp
ENST00000649408.2:c.3015G>T ENSP00000497386.2:p.Glu1005Asp
ENST00000649724.1:c.2130G>T ENSP00000497932.1:p.Glu710Asp
ENST00000649749.1:c.2130G>T ENSP00000497210.1:p.Glu710Asp
ENST00000679375.1:c.*1247G>T ENSP00000505887.1:n.*1247G>T
ENST00000679465.1:n.3468G>T
ENST00000679805.1:n.3343G>T
ENST00000679899.1:c.2073G>T ENSP00000505996.1:p.Glu691Asp
ENST00000680270.1:c.2130G>T ENSP00000505532.1:p.Glu710Asp
ENST00000680305.1:c.3015G>T ENSP00000506312.1:p.Glu1005Asp
ENST00000681056.1:c.2130G>T ENSP00000506234.1:p.Glu710Asp
ENST00000681235.1:c.*2537G>T ENSP00000506606.1:n.*2537G>T
ENST00000681429.1:n.2275G>T
ENST00000681683.1:c.2130G>T ENSP00000506666.1:p.Glu710Asp
ENST00000681786.1:n.3468G>T
ENST00000681901.1:c.*2615G>T ENSP00000504883.1:n.*2615G>T
ENST00000368471.7:c.2130G>T ENSP00000357456.3:p.Glu710Asp
ENST00000368474.8:c.3015G>T ENSP00000357459.4:p.Glu1005Asp
ENST00000529168.1:c.2922G>T ENSP00000431794.1:p.Glu974Asp
ENST00000530954.1:n.152G>T
ENST00000534279.1:n.474G>T
NM_001025107.2:c.2130G>T NP_001020278.1:p.Glu710Asp
NM_001111.4:c.3015G>T NP_001102.2:p.Glu1005Asp
NM_001193495.1:c.2130G>T NP_001180424.1:p.Glu710Asp
NM_015840.3:c.2937G>T NP_056655.2:p.Glu979Asp
NM_015841.3:c.2880G>T NP_056656.2:p.Glu960Asp
XM_006711109.1:c.3045G>T XP_006711172.1:p.Glu1015Asp
XM_006711111.2:c.2130G>T XP_006711174.1:p.Glu710Asp
XM_006711112.1:c.2130G>T XP_006711175.1:p.Glu710Asp
XM_006711113.1:c.2130G>T XP_006711176.1:p.Glu710Asp
XM_011509060.1:c.3144G>T XP_011507362.1:p.Glu1048Asp
XM_011509061.1:c.3066G>T XP_011507363.1:p.Glu1022Asp
XM_011509062.1:c.3033G>T XP_011507364.1:p.Glu1011Asp
NM_001025107.3:c.2130G>T NP_001020278.1:p.Glu710Asp
NM_001111.5:c.3015G>T MANE Select NP_001102.3:p.Glu1005Asp
NM_001193495.2:c.2130G>T NP_001180424.1:p.Glu710Asp
NM_001365045.1:c.3042G>T NP_001351974.1:p.Glu1014Asp
NM_001365046.1:c.2130G>T NP_001351975.1:p.Glu710Asp
NM_001365047.1:c.2130G>T NP_001351976.1:p.Glu710Asp
NM_001365048.1:c.2130G>T NP_001351977.1:p.Glu710Asp
NM_001365049.1:c.2052G>T NP_001351978.1:p.Glu684Asp
NM_015840.4:c.2937G>T NP_056655.3:p.Glu979Asp
NM_015841.4:c.2880G>T NP_056656.3:p.Glu960Asp
XM_006711113.2:c.2130G>T XP_006711176.1:p.Glu710Asp
XM_011509061.2:c.2052G>T XP_011507363.2:p.Glu684Asp
XM_024449674.1:c.3144G>T XP_024305442.1:p.Glu1048Asp