Canonical Allele Identifier: CA2365854466

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620093C= , CM000682.2:g.44620093C= GRCh38
NC_000020.10:g.43248734C= , CM000682.1:g.43248734C= GRCh37
NC_000020.9:g.42682148C= NCBI36
NG_007385.1:g.36643G= , LRG_16:g.36643G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.1245+206G= (ADA)
ENST00000536076.2:c.925+206G= (ADA) ENSP00000512234.1:n.925+206G=
ENST00000536532.6:c.*221+206G= (ADA) ENSP00000440946.1:n.*221+206G=
ENST00000537820.2:c.1006+206G= (ADA) ENSP00000441818.1:n.1006+206G=
ENST00000539235.6:c.*462+206G= (ADA) ENSP00000446464.1:n.*462+206G=
ENST00000695889.1:c.553+206G= (ADA) ENSP00000512240.1:n.553+206G=
ENST00000695890.1:n.5395G= (ADA)
ENST00000695891.1:c.618+206G= (ADA) ENSP00000512241.1:n.618+206G=
ENST00000695927.1:c.1156+206G= (ADA) ENSP00000512270.1:n.1156+206G=
ENST00000695949.1:c.1003+206G= (ADA) ENSP00000512281.1:n.1003+206G=
ENST00000695956.1:c.233+206G= (ADA)
ENST00000695957.1:c.*569+206G= (ADA) ENSP00000512286.1:n.*569+206G=
ENST00000695991.1:c.616+206G= (ADA) ENSP00000512314.1:n.616+206G=
ENST00000695992.1:c.*427G= (ADA) ENSP00000512315.1:n.*427G=
ENST00000695993.1:c.1079-148G= (ADA) ENSP00000512316.1:n.1079-148G=
ENST00000695994.1:c.*221+206G= (ADA) ENSP00000512317.1:n.*221+206G=
ENST00000695995.1:c.688+206G= (ADA) ENSP00000512318.1:n.688+206G=
ENST00000695996.1:n.1160+206G= (ADA)
ENST00000696003.1:n.2862+206G= (ADA)
ENST00000696004.1:n.2068G= (ADA)
ENST00000696005.1:c.734G= (ADA)
ENST00000696006.1:c.*221+206G= (ADA) ENSP00000512325.1:n.*221+206G=
ENST00000696007.1:c.1005+206G= (ADA) ENSP00000512326.1:n.1005+206G=
ENST00000696008.1:n.3638G= (ADA)
ENST00000696017.1:c.*27G= (ADA) ENSP00000512333.1:n.*27G=
ENST00000696034.1:c.*221+206G= (ADA) ENSP00000512343.1:n.*221+206G=
ENST00000696035.1:n.1470G= (ADA)
ENST00000696036.1:n.1985G= (ADA)
ENST00000696037.1:n.2755+206G= (ADA)
ENST00000696038.1:c.*1041G= (ADA) ENSP00000512344.1:n.*1041G=
ENST00000696039.1:n.1442+206G= (ADA)
ENST00000696058.1:c.1076-148G= (ADA) ENSP00000512361.1:n.1076-148G=
ENST00000696059.1:c.*1023+206G= (ADA) ENSP00000512362.1:n.*1023+206G=
ENST00000696060.1:c.1147+206G= (ADA) ENSP00000512363.1:n.1147+206G=
ENST00000696061.1:c.1075+206G= (ADA) ENSP00000512364.1:n.1075+206G=
ENST00000696062.1:c.1141+206G= (ADA) ENSP00000512365.1:n.1141+206G=
ENST00000696063.1:c.1153+206G= (ADA) ENSP00000512366.1:n.1153+206G=
ENST00000696064.1:c.925+206G= (ADA) ENSP00000512367.1:n.925+206G=
ENST00000696065.1:c.400+206G= (ADA) ENSP00000512368.1:n.400+206G=
ENST00000696072.1:n.639G= (ADA)
ENST00000696073.1:n.1389+206G= (ADA)
ENST00000696074.1:n.629+206G= (ADA)
ENST00000696075.1:c.*1048+206G= (ADA) ENSP00000512374.1:n.*1048+206G=
ENST00000696076.1:c.*27G= (ADA) ENSP00000512375.1:n.*27G=
ENST00000696077.1:c.1072+206G= (ADA) ENSP00000512376.1:n.1072+206G=
ENST00000696078.1:c.1075+206G= (ADA) ENSP00000512377.1:n.1075+206G=
ENST00000696079.1:c.1075+206G= (ADA) ENSP00000512378.1:n.1075+206G=
ENST00000696080.1:c.1078+206G= (ADA) ENSP00000512379.1:n.1078+206G=
ENST00000696081.1:n.1403G= (ADA)
ENST00000696082.1:c.1153+206G= (ADA) ENSP00000512380.1:n.1153+206G=
ENST00000696083.1:n.2035+206G= (ADA)
ENST00000696084.1:n.1461G= (ADA)
ENST00000696104.1:c.*147+206G= (ADA) ENSP00000512399.1:n.*147+206G=
ENST00000372874.9:c.1078+206G= (ADA) MANE Select ENSP00000361965.4:n.1078+206G=
ENST00000372874.8:c.1078+206G= (ADA) ENSP00000361965.4:n.1078+206G=
ENST00000372887.5:c.152-3840C= (PKIG) ENSP00000361978.1:n.152-3840C=
ENST00000464097.5:n.1444+206G= (ADA)
ENST00000492931.5:n.1238+206G= (ADA)
ENST00000536532.5:c.*221+206G= (ADA) ENSP00000440946.1:n.*221+206G=
ENST00000537820.1:c.1006+206G= (ADA) ENSP00000441818.1:n.1006+206G=
ENST00000539235.5:c.*462+206G= (ADA) ENSP00000446464.1:n.*462+206G=
NM_000022.2:c.1078+206G= , LRG_16t1:c.1078+206G= (ADA) NP_000013.2:n.1078+206G=
XM_005260236.2:c.1006+206G= (ADA) XP_005260293.1:n.1006+206G=
XM_011528478.1:c.673+206G= (ADA) XP_011526780.1:n.673+206G=
XM_011528479.1:c.673+206G= (ADA) XP_011526781.1:n.673+206G=
XR_244129.1:n.1067+206G= (ADA)
NM_000022.3:c.1078+206G= (ADA) NP_000013.2:n.1078+206G=
NM_001322050.1:c.673+206G= (ADA) NP_001308979.1:n.673+206G=
NM_001322051.1:c.1006+206G= (ADA) NP_001308980.1:n.1006+206G=
NR_136160.1:n.1164+206G= (ADA)
NM_000022.4:c.1078+206G= (ADA) MANE Select NP_000013.2:n.1078+206G=
NM_001322050.2:c.673+206G= (ADA) NP_001308979.1:n.673+206G=
NM_001322051.2:c.1006+206G= (ADA) NP_001308980.1:n.1006+206G=
NR_136160.2:n.1105+206G= (ADA)