Canonical Allele Identifier: CA342596171
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154601155A>T , CM000663.2:g.154601155A>T GRCh38
NC_000001.10:g.154573631A>T , CM000663.1:g.154573631A>T GRCh37
NC_000001.9:g.152840255A>T NCBI36
NG_011844.1:g.31807T>A
NG_011844.2:g.35406T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.1381T>A ENSP00000497790.2:n.1381T>A
ENST00000649724.2:c.1517T>A ENSP00000497932.2:p.Leu506Gln
ENST00000680270.2:c.1370T>A ENSP00000505532.2:p.Leu457Gln
ENST00000681056.2:c.1139T>A ENSP00000506234.2:p.Leu380Gln
ENST00000368471.8:c.602T>A ENSP00000357456.3:p.Leu201Gln
ENST00000368474.9:c.1487T>A MANE Select ENSP00000357459.4:p.Leu496Gln
ENST00000529168.2:c.1487T>A ENSP00000431794.2:p.Leu496Gln
ENST00000647682.2:n.1217T>A
ENST00000648231.2:c.602T>A ENSP00000497555.1:p.Leu201Gln
ENST00000648311.1:c.602T>A ENSP00000498137.1:p.Leu201Gln
ENST00000648714.2:c.1487T>A ENSP00000497434.2:p.Leu496Gln
ENST00000648871.1:c.602T>A ENSP00000497793.1:p.Leu201Gln
ENST00000649021.1:n.1523T>A
ENST00000649022.2:c.602T>A ENSP00000496896.2:p.Leu201Gln
ENST00000649042.1:c.602T>A ENSP00000497790.1:p.Leu201Gln
ENST00000649408.2:c.1487T>A ENSP00000497386.2:p.Leu496Gln
ENST00000649724.1:c.602T>A ENSP00000497932.1:p.Leu201Gln
ENST00000649749.1:c.602T>A ENSP00000497210.1:p.Leu201Gln
ENST00000679375.1:c.602T>A ENSP00000505887.1:p.Leu201Gln
ENST00000679465.1:n.1685T>A
ENST00000679805.1:n.1523T>A
ENST00000679899.1:c.602T>A ENSP00000505996.1:p.Leu201Gln
ENST00000680270.1:c.602T>A ENSP00000505532.1:p.Leu201Gln
ENST00000680305.1:c.1487T>A ENSP00000506312.1:p.Leu496Gln
ENST00000680472.1:n.1526T>A
ENST00000681056.1:c.602T>A ENSP00000506234.1:p.Leu201Gln
ENST00000681235.1:c.*1087T>A ENSP00000506606.1:n.*1087T>A
ENST00000681683.1:c.602T>A ENSP00000506666.1:p.Leu201Gln
ENST00000681786.1:n.1685T>A
ENST00000681901.1:c.*1087T>A ENSP00000504883.1:n.*1087T>A
ENST00000368471.7:c.602T>A ENSP00000357456.3:p.Leu201Gln
ENST00000368474.8:c.1487T>A ENSP00000357459.4:p.Leu496Gln
ENST00000463920.5:n.1369T>A
ENST00000529168.1:c.1472T>A ENSP00000431794.1:p.Leu491Gln
NM_001025107.2:c.602T>A NP_001020278.1:p.Leu201Gln
NM_001111.4:c.1487T>A NP_001102.2:p.Leu496Gln
NM_001193495.1:c.602T>A NP_001180424.1:p.Leu201Gln
NM_015840.3:c.1487T>A NP_056655.2:p.Leu496Gln
NM_015841.3:c.1487T>A NP_056656.2:p.Leu496Gln
XM_006711109.1:c.1517T>A XP_006711172.1:p.Leu506Gln
XM_006711111.2:c.602T>A XP_006711174.1:p.Leu201Gln
XM_006711112.1:c.602T>A XP_006711175.1:p.Leu201Gln
XM_006711113.1:c.602T>A XP_006711176.1:p.Leu201Gln
XM_011509060.1:c.1616T>A XP_011507362.1:p.Leu539Gln
XM_011509061.1:c.1616T>A XP_011507363.1:p.Leu539Gln
XM_011509062.1:c.1505T>A XP_011507364.1:p.Leu502Gln
NM_001025107.3:c.602T>A NP_001020278.1:p.Leu201Gln
NM_001111.5:c.1487T>A MANE Select NP_001102.3:p.Leu496Gln
NM_001193495.2:c.602T>A NP_001180424.1:p.Leu201Gln
NM_001365045.1:c.1514T>A NP_001351974.1:p.Leu505Gln
NM_001365046.1:c.602T>A NP_001351975.1:p.Leu201Gln
NM_001365047.1:c.602T>A NP_001351976.1:p.Leu201Gln
NM_001365048.1:c.602T>A NP_001351977.1:p.Leu201Gln
NM_001365049.1:c.602T>A NP_001351978.1:p.Leu201Gln
NM_015840.4:c.1487T>A NP_056655.3:p.Leu496Gln
NM_015841.4:c.1487T>A NP_056656.3:p.Leu496Gln
XM_006711113.2:c.602T>A XP_006711176.1:p.Leu201Gln
XM_011509061.2:c.602T>A XP_011507363.2:p.Leu201Gln
XM_024449674.1:c.1616T>A XP_024305442.1:p.Leu539Gln