Canonical Allele Identifier: CA2365854437

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620037A= , CM000682.2:g.44620037A= GRCh38
NC_000020.10:g.43248678A= , CM000682.1:g.43248678A= GRCh37
NC_000020.9:g.42682092A= NCBI36
NG_007385.1:g.36699T= , LRG_16:g.36699T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.1246-190T= (ADA)
ENST00000536076.2:c.926-190T= (ADA) ENSP00000512234.1:n.926-190T=
ENST00000536532.6:c.*222-190T= (ADA) ENSP00000440946.1:n.*222-190T=
ENST00000537820.2:c.1007-190T= (ADA) ENSP00000441818.1:n.1007-190T=
ENST00000539235.6:c.*463-190T= (ADA) ENSP00000446464.1:n.*463-190T=
ENST00000695889.1:c.554-190T= (ADA) ENSP00000512240.1:n.554-190T=
ENST00000695890.1:n.5451T= (ADA)
ENST00000695891.1:c.619-190T= (ADA) ENSP00000512241.1:n.619-190T=
ENST00000695927.1:c.1157-190T= (ADA) ENSP00000512270.1:n.1157-190T=
ENST00000695949.1:c.1004-190T= (ADA) ENSP00000512281.1:n.1004-190T=
ENST00000695956.1:c.234-177T= (ADA)
ENST00000695957.1:c.*570-190T= (ADA) ENSP00000512286.1:n.*570-190T=
ENST00000695991.1:c.617-190T= (ADA) ENSP00000512314.1:n.617-190T=
ENST00000695992.1:c.*483T= (ADA) ENSP00000512315.1:n.*483T=
ENST00000695993.1:c.1079-92T= (ADA) ENSP00000512316.1:n.1079-92T=
ENST00000695994.1:c.*222-190T= (ADA) ENSP00000512317.1:n.*222-190T=
ENST00000695995.1:c.689-190T= (ADA) ENSP00000512318.1:n.689-190T=
ENST00000695996.1:n.1161-190T= (ADA)
ENST00000696003.1:n.2863-190T= (ADA)
ENST00000696004.1:n.2124T= (ADA)
ENST00000696005.1:c.790T= (ADA)
ENST00000696006.1:c.*222-190T= (ADA) ENSP00000512325.1:n.*222-190T=
ENST00000696007.1:c.1006-190T= (ADA) ENSP00000512326.1:n.1006-190T=
ENST00000696008.1:n.3694T= (ADA)
ENST00000696017.1:c.*83T= (ADA) ENSP00000512333.1:n.*83T=
ENST00000696034.1:c.*221+262T= (ADA) ENSP00000512343.1:n.*221+262T=
ENST00000696035.1:n.1526T= (ADA)
ENST00000696036.1:n.2041T= (ADA)
ENST00000696037.1:n.2756-190T= (ADA)
ENST00000696038.1:c.*1097T= (ADA) ENSP00000512344.1:n.*1097T=
ENST00000696039.1:n.1443-190T= (ADA)
ENST00000696058.1:c.1076-92T= (ADA) ENSP00000512361.1:n.1076-92T=
ENST00000696059.1:c.*1024-190T= (ADA) ENSP00000512362.1:n.*1024-190T=
ENST00000696060.1:c.1148-190T= (ADA) ENSP00000512363.1:n.1148-190T=
ENST00000696061.1:c.1076-190T= (ADA) ENSP00000512364.1:n.1076-190T=
ENST00000696062.1:c.1142-190T= (ADA) ENSP00000512365.1:n.1142-190T=
ENST00000696063.1:c.1154-190T= (ADA) ENSP00000512366.1:n.1154-190T=
ENST00000696064.1:c.926-190T= (ADA) ENSP00000512367.1:n.926-190T=
ENST00000696065.1:c.401-190T= (ADA) ENSP00000512368.1:n.401-190T=
ENST00000696072.1:n.695T= (ADA)
ENST00000696073.1:n.1390-190T= (ADA)
ENST00000696074.1:n.630-190T= (ADA)
ENST00000696075.1:c.*1049-190T= (ADA) ENSP00000512374.1:n.*1049-190T=
ENST00000696076.1:c.*83T= (ADA) ENSP00000512375.1:n.*83T=
ENST00000696077.1:c.1073-190T= (ADA) ENSP00000512376.1:n.1073-190T=
ENST00000696078.1:c.1076-190T= (ADA) ENSP00000512377.1:n.1076-190T=
ENST00000696079.1:c.1076-195T= (ADA) ENSP00000512378.1:n.1076-195T=
ENST00000696080.1:c.1079-195T= (ADA) ENSP00000512379.1:n.1079-195T=
ENST00000696081.1:n.1459T= (ADA)
ENST00000696082.1:c.1154-190T= (ADA) ENSP00000512380.1:n.1154-190T=
ENST00000696083.1:n.2036-190T= (ADA)
ENST00000696084.1:n.1517T= (ADA)
ENST00000696104.1:c.*148-190T= (ADA) ENSP00000512399.1:n.*148-190T=
ENST00000372874.9:c.1079-190T= (ADA) MANE Select ENSP00000361965.4:n.1079-190T=
ENST00000372874.8:c.1079-190T= (ADA) ENSP00000361965.4:n.1079-190T=
ENST00000372887.5:c.152-3896A= (PKIG) ENSP00000361978.1:n.152-3896A=
ENST00000464097.5:n.1445-190T= (ADA)
ENST00000492931.5:n.1239-190T= (ADA)
ENST00000536532.5:c.*222-190T= (ADA) ENSP00000440946.1:n.*222-190T=
ENST00000537820.1:c.1007-190T= (ADA) ENSP00000441818.1:n.1007-190T=
ENST00000539235.5:c.*463-190T= (ADA) ENSP00000446464.1:n.*463-190T=
NM_000022.2:c.1079-190T= , LRG_16t1:c.1079-190T= (ADA) NP_000013.2:n.1079-190T=
XM_005260236.2:c.1007-190T= (ADA) XP_005260293.1:n.1007-190T=
XM_011528478.1:c.674-190T= (ADA) XP_011526780.1:n.674-190T=
XM_011528479.1:c.674-190T= (ADA) XP_011526781.1:n.674-190T=
XR_244129.1:n.1068-190T= (ADA)
NM_000022.3:c.1079-190T= (ADA) NP_000013.2:n.1079-190T=
NM_001322050.1:c.674-190T= (ADA) NP_001308979.1:n.674-190T=
NM_001322051.1:c.1007-190T= (ADA) NP_001308980.1:n.1007-190T=
NR_136160.1:n.1165-190T= (ADA)
NM_000022.4:c.1079-190T= (ADA) MANE Select NP_000013.2:n.1079-190T=
NM_001322050.2:c.674-190T= (ADA) NP_001308979.1:n.674-190T=
NM_001322051.2:c.1007-190T= (ADA) NP_001308980.1:n.1007-190T=
NR_136160.2:n.1106-190T= (ADA)