Canonical Allele Identifier: CA2365856545

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624232G= , CM000682.2:g.44624232G= GRCh38
NC_000020.10:g.43252873G= , CM000682.1:g.43252873G= GRCh37
NC_000020.9:g.42686287G= NCBI36
NG_007385.1:g.32504C= , LRG_16:g.32504C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.667C= (ADA)
ENST00000536076.2:c.423C= (ADA) ENSP00000512234.1:p.Ser141=
ENST00000536532.6:c.576C= (ADA) ENSP00000440946.1:p.Ser192=
ENST00000537820.2:c.576C= (ADA) ENSP00000441818.1:p.Ser192=
ENST00000539235.6:c.219-1154C= (ADA) ENSP00000446464.1:n.219-1154C=
ENST00000695889.1:c.219-1302C= (ADA) ENSP00000512240.1:n.219-1302C=
ENST00000695890.1:n.2379C= (ADA)
ENST00000695891.1:c.219-1302C= (ADA) ENSP00000512241.1:n.219-1302C=
ENST00000695927.1:c.654C= (ADA) ENSP00000512270.1:p.Ser218=
ENST00000695949.1:c.573C= (ADA) ENSP00000512281.1:p.Ser191=
ENST00000695957.1:c.*67C= (ADA) ENSP00000512286.1:n.*67C=
ENST00000695991.1:c.217-1302C= (ADA) ENSP00000512314.1:n.217-1302C=
ENST00000695992.1:c.576C= (ADA) ENSP00000512315.1:p.Ser192=
ENST00000695993.1:c.576C= (ADA) ENSP00000512316.1:p.Ser192=
ENST00000695994.1:c.576C= (ADA) ENSP00000512317.1:p.Ser192=
ENST00000695995.1:c.217-1154C= (ADA) ENSP00000512318.1:n.217-1154C=
ENST00000695996.1:n.647C= (ADA)
ENST00000695997.1:n.531C= (ADA)
ENST00000696003.1:n.668C= (ADA)
ENST00000696004.1:n.668C= (ADA)
ENST00000696005.1:c.98C= (ADA)
ENST00000696006.1:c.576C= (ADA) ENSP00000512325.1:p.Ser192=
ENST00000696007.1:c.427C= (ADA) ENSP00000512326.1:n.427C=
ENST00000696008.1:n.1731C= (ADA)
ENST00000696009.1:n.1926C= (ADA)
ENST00000696017.1:c.573C= (ADA) ENSP00000512333.1:p.Ser191=
ENST00000696034.1:c.576C= (ADA) ENSP00000512343.1:p.Ser192=
ENST00000696035.1:n.686C= (ADA)
ENST00000696036.1:n.1266C= (ADA)
ENST00000696037.1:n.2253C= (ADA)
ENST00000696038.1:c.*322C= (ADA) ENSP00000512344.1:n.*322C=
ENST00000696039.1:n.864C= (ADA)
ENST00000696058.1:c.576C= (ADA) ENSP00000512361.1:p.Ser192=
ENST00000696059.1:c.*521C= (ADA) ENSP00000512362.1:n.*521C=
ENST00000696060.1:c.576C= (ADA) ENSP00000512363.1:p.Ser192=
ENST00000696061.1:c.573C= (ADA) ENSP00000512364.1:p.Ser191=
ENST00000696062.1:c.639C= (ADA) ENSP00000512365.1:p.Ser213=
ENST00000696063.1:c.651C= (ADA) ENSP00000512366.1:p.Ser217=
ENST00000696064.1:c.423C= (ADA) ENSP00000512367.1:p.Ser141=
ENST00000696065.1:c.66-1302C= (ADA) ENSP00000512368.1:n.66-1302C=
ENST00000696074.1:n.192C= (ADA)
ENST00000696075.1:c.*546C= (ADA) ENSP00000512374.1:n.*546C=
ENST00000696076.1:c.576C= (ADA) ENSP00000512375.1:p.Ser192=
ENST00000696077.1:c.573C= (ADA) ENSP00000512376.1:p.Ser191=
ENST00000696078.1:c.576C= (ADA) ENSP00000512377.1:p.Ser192=
ENST00000696079.1:c.576C= (ADA) ENSP00000512378.1:p.Ser192=
ENST00000696080.1:c.576C= (ADA) ENSP00000512379.1:p.Ser192=
ENST00000696081.1:n.695C= (ADA)
ENST00000696082.1:c.654C= (ADA) ENSP00000512380.1:p.Ser218=
ENST00000696083.1:n.1457C= (ADA)
ENST00000696084.1:n.677C= (ADA)
ENST00000696104.1:c.363-1302C= (ADA) ENSP00000512399.1:n.363-1302C=
ENST00000696105.1:c.*117C= (ADA) ENSP00000512400.1:n.*117C=
ENST00000372874.9:c.576C= (ADA) MANE Select ENSP00000361965.4:p.Ser192=
ENST00000372874.8:c.576C= (ADA) ENSP00000361965.4:p.Ser192=
ENST00000372887.5:c.*256G= (PKIG) ENSP00000361978.1:n.*256G=
ENST00000464097.5:n.250C= (ADA)
ENST00000492931.5:n.660C= (ADA)
ENST00000536532.5:c.576C= (ADA) ENSP00000440946.1:p.Ser192=
ENST00000537820.1:c.576C= (ADA) ENSP00000441818.1:p.Ser192=
ENST00000539235.5:c.219-1154C= (ADA) ENSP00000446464.1:n.219-1154C=
NM_000022.2:c.576C= , LRG_16t1:c.576C= (ADA) NP_000013.2:p.Ser192=
XM_005260236.2:c.576C= (ADA) XP_005260293.1:p.Ser192=
XM_011528478.1:c.171C= (ADA) XP_011526780.1:p.Ser57=
XM_011528479.1:c.171C= (ADA) XP_011526781.1:p.Ser57=
XR_244129.1:n.630C= (ADA)
NM_000022.3:c.576C= (ADA) NP_000013.2:p.Ser192=
NM_001322050.1:c.171C= (ADA) NP_001308979.1:p.Ser57=
NM_001322051.1:c.576C= (ADA) NP_001308980.1:p.Ser192=
NR_136160.1:n.727C= (ADA)
NM_000022.4:c.576C= (ADA) MANE Select NP_000013.2:p.Ser192=
NM_001322050.2:c.171C= (ADA) NP_001308979.1:p.Ser57=
NM_001322051.2:c.576C= (ADA) NP_001308980.1:p.Ser192=
NR_136160.2:n.668C= (ADA)