Canonical Allele Identifier: CA2365854453

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620056A= , CM000682.2:g.44620056A= GRCh38
NC_000020.10:g.43248697A= , CM000682.1:g.43248697A= GRCh37
NC_000020.9:g.42682111A= NCBI36
NG_007385.1:g.36680T= , LRG_16:g.36680T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.1246-209T= (ADA)
ENST00000536076.2:c.926-209T= (ADA) ENSP00000512234.1:n.926-209T=
ENST00000536532.6:c.*222-209T= (ADA) ENSP00000440946.1:n.*222-209T=
ENST00000537820.2:c.1007-209T= (ADA) ENSP00000441818.1:n.1007-209T=
ENST00000539235.6:c.*463-209T= (ADA) ENSP00000446464.1:n.*463-209T=
ENST00000695889.1:c.554-209T= (ADA) ENSP00000512240.1:n.554-209T=
ENST00000695890.1:n.5432T= (ADA)
ENST00000695891.1:c.619-209T= (ADA) ENSP00000512241.1:n.619-209T=
ENST00000695927.1:c.1157-209T= (ADA) ENSP00000512270.1:n.1157-209T=
ENST00000695949.1:c.1004-209T= (ADA) ENSP00000512281.1:n.1004-209T=
ENST00000695956.1:c.234-196T= (ADA)
ENST00000695957.1:c.*570-209T= (ADA) ENSP00000512286.1:n.*570-209T=
ENST00000695991.1:c.617-209T= (ADA) ENSP00000512314.1:n.617-209T=
ENST00000695992.1:c.*464T= (ADA) ENSP00000512315.1:n.*464T=
ENST00000695993.1:c.1079-111T= (ADA) ENSP00000512316.1:n.1079-111T=
ENST00000695994.1:c.*222-209T= (ADA) ENSP00000512317.1:n.*222-209T=
ENST00000695995.1:c.689-209T= (ADA) ENSP00000512318.1:n.689-209T=
ENST00000695996.1:n.1161-209T= (ADA)
ENST00000696003.1:n.2863-209T= (ADA)
ENST00000696004.1:n.2105T= (ADA)
ENST00000696005.1:c.771T= (ADA)
ENST00000696006.1:c.*222-209T= (ADA) ENSP00000512325.1:n.*222-209T=
ENST00000696007.1:c.1006-209T= (ADA) ENSP00000512326.1:n.1006-209T=
ENST00000696008.1:n.3675T= (ADA)
ENST00000696017.1:c.*64T= (ADA) ENSP00000512333.1:n.*64T=
ENST00000696034.1:c.*221+243T= (ADA) ENSP00000512343.1:n.*221+243T=
ENST00000696035.1:n.1507T= (ADA)
ENST00000696036.1:n.2022T= (ADA)
ENST00000696037.1:n.2756-209T= (ADA)
ENST00000696038.1:c.*1078T= (ADA) ENSP00000512344.1:n.*1078T=
ENST00000696039.1:n.1443-209T= (ADA)
ENST00000696058.1:c.1076-111T= (ADA) ENSP00000512361.1:n.1076-111T=
ENST00000696059.1:c.*1024-209T= (ADA) ENSP00000512362.1:n.*1024-209T=
ENST00000696060.1:c.1148-209T= (ADA) ENSP00000512363.1:n.1148-209T=
ENST00000696061.1:c.1076-209T= (ADA) ENSP00000512364.1:n.1076-209T=
ENST00000696062.1:c.1142-209T= (ADA) ENSP00000512365.1:n.1142-209T=
ENST00000696063.1:c.1154-209T= (ADA) ENSP00000512366.1:n.1154-209T=
ENST00000696064.1:c.926-209T= (ADA) ENSP00000512367.1:n.926-209T=
ENST00000696065.1:c.401-209T= (ADA) ENSP00000512368.1:n.401-209T=
ENST00000696072.1:n.676T= (ADA)
ENST00000696073.1:n.1390-209T= (ADA)
ENST00000696074.1:n.630-209T= (ADA)
ENST00000696075.1:c.*1049-209T= (ADA) ENSP00000512374.1:n.*1049-209T=
ENST00000696076.1:c.*64T= (ADA) ENSP00000512375.1:n.*64T=
ENST00000696077.1:c.1073-209T= (ADA) ENSP00000512376.1:n.1073-209T=
ENST00000696078.1:c.1076-209T= (ADA) ENSP00000512377.1:n.1076-209T=
ENST00000696079.1:c.1076-214T= (ADA) ENSP00000512378.1:n.1076-214T=
ENST00000696080.1:c.1079-214T= (ADA) ENSP00000512379.1:n.1079-214T=
ENST00000696081.1:n.1440T= (ADA)
ENST00000696082.1:c.1154-209T= (ADA) ENSP00000512380.1:n.1154-209T=
ENST00000696083.1:n.2036-209T= (ADA)
ENST00000696084.1:n.1498T= (ADA)
ENST00000696104.1:c.*148-209T= (ADA) ENSP00000512399.1:n.*148-209T=
ENST00000372874.9:c.1079-209T= (ADA) MANE Select ENSP00000361965.4:n.1079-209T=
ENST00000372874.8:c.1079-209T= (ADA) ENSP00000361965.4:n.1079-209T=
ENST00000372887.5:c.152-3877A= (PKIG) ENSP00000361978.1:n.152-3877A=
ENST00000464097.5:n.1445-209T= (ADA)
ENST00000492931.5:n.1239-209T= (ADA)
ENST00000536532.5:c.*222-209T= (ADA) ENSP00000440946.1:n.*222-209T=
ENST00000537820.1:c.1007-209T= (ADA) ENSP00000441818.1:n.1007-209T=
ENST00000539235.5:c.*463-209T= (ADA) ENSP00000446464.1:n.*463-209T=
NM_000022.2:c.1079-209T= , LRG_16t1:c.1079-209T= (ADA) NP_000013.2:n.1079-209T=
XM_005260236.2:c.1007-209T= (ADA) XP_005260293.1:n.1007-209T=
XM_011528478.1:c.674-209T= (ADA) XP_011526780.1:n.674-209T=
XM_011528479.1:c.674-209T= (ADA) XP_011526781.1:n.674-209T=
XR_244129.1:n.1068-209T= (ADA)
NM_000022.3:c.1079-209T= (ADA) NP_000013.2:n.1079-209T=
NM_001322050.1:c.674-209T= (ADA) NP_001308979.1:n.674-209T=
NM_001322051.1:c.1007-209T= (ADA) NP_001308980.1:n.1007-209T=
NR_136160.1:n.1165-209T= (ADA)
NM_000022.4:c.1079-209T= (ADA) MANE Select NP_000013.2:n.1079-209T=
NM_001322050.2:c.674-209T= (ADA) NP_001308979.1:n.674-209T=
NM_001322051.2:c.1007-209T= (ADA) NP_001308980.1:n.1007-209T=
NR_136160.2:n.1106-209T= (ADA)