Canonical Allele Identifier: CA2365855877

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44622898T= , CM000682.2:g.44622898T= GRCh38
NC_000020.10:g.43251539T= , CM000682.1:g.43251539T= GRCh37
NC_000020.9:g.42684953T= NCBI36
NG_007385.1:g.33838A= , LRG_16:g.33838A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.878A= (ADA)
ENST00000536076.2:c.558A= (ADA) ENSP00000512234.1:p.Gly186=
ENST00000536532.6:c.711A= (ADA) ENSP00000440946.1:p.Gly237=
ENST00000537820.2:c.639A= (ADA) ENSP00000441818.1:p.Gly213=
ENST00000539235.6:c.*95A= (ADA) ENSP00000446464.1:n.*95A=
ENST00000695889.1:c.251A= (ADA) ENSP00000512240.1:p.Asp84=
ENST00000695890.1:n.2590A= (ADA)
ENST00000695891.1:c.251A= (ADA) ENSP00000512241.1:p.Asp84=
ENST00000695927.1:c.789A= (ADA) ENSP00000512270.1:p.Gly263=
ENST00000695949.1:c.636A= (ADA) ENSP00000512281.1:p.Gly212=
ENST00000695957.1:c.*202A= (ADA) ENSP00000512286.1:n.*202A=
ENST00000695991.1:c.249A= (ADA) ENSP00000512314.1:p.Gly83=
ENST00000695992.1:c.711A= (ADA) ENSP00000512315.1:p.Gly237=
ENST00000695993.1:c.711A= (ADA) ENSP00000512316.1:p.Gly237=
ENST00000695994.1:c.684A= (ADA) ENSP00000512317.1:p.Gly228=
ENST00000695995.1:c.321A= (ADA) ENSP00000512318.1:p.Gly107=
ENST00000695996.1:n.858A= (ADA)
ENST00000696003.1:n.879A= (ADA)
ENST00000696004.1:n.879A= (ADA)
ENST00000696005.1:c.161A= (ADA)
ENST00000696006.1:c.639A= (ADA) ENSP00000512325.1:p.Gly213=
ENST00000696007.1:c.638A= (ADA) ENSP00000512326.1:n.638A=
ENST00000696008.1:n.3065A= (ADA)
ENST00000696017.1:c.708A= (ADA) ENSP00000512333.1:p.Gly236=
ENST00000696034.1:c.711A= (ADA) ENSP00000512343.1:p.Gly237=
ENST00000696035.1:n.897A= (ADA)
ENST00000696036.1:n.1477A= (ADA)
ENST00000696037.1:n.2388A= (ADA)
ENST00000696038.1:c.*533A= (ADA) ENSP00000512344.1:n.*533A=
ENST00000696039.1:n.1075A= (ADA)
ENST00000696058.1:c.708A= (ADA) ENSP00000512361.1:p.Gly236=
ENST00000696059.1:c.*656A= (ADA) ENSP00000512362.1:n.*656A=
ENST00000696060.1:c.780A= (ADA) ENSP00000512363.1:p.Gly260=
ENST00000696061.1:c.708A= (ADA) ENSP00000512364.1:p.Gly236=
ENST00000696062.1:c.774A= (ADA) ENSP00000512365.1:p.Gly258=
ENST00000696063.1:c.786A= (ADA) ENSP00000512366.1:p.Gly262=
ENST00000696064.1:c.558A= (ADA) ENSP00000512367.1:p.Gly186=
ENST00000696065.1:c.98A= (ADA) ENSP00000512368.1:p.Asp33=
ENST00000696073.1:n.1022A= (ADA)
ENST00000696074.1:n.327A= (ADA)
ENST00000696075.1:c.*681A= (ADA) ENSP00000512374.1:n.*681A=
ENST00000696076.1:c.780A= (ADA) ENSP00000512375.1:p.Gly260=
ENST00000696077.1:c.705A= (ADA) ENSP00000512376.1:p.Gly235=
ENST00000696078.1:c.708A= (ADA) ENSP00000512377.1:p.Gly236=
ENST00000696079.1:c.708A= (ADA) ENSP00000512378.1:p.Gly236=
ENST00000696080.1:c.711A= (ADA) ENSP00000512379.1:p.Gly237=
ENST00000696081.1:n.830A= (ADA)
ENST00000696082.1:c.786A= (ADA) ENSP00000512380.1:p.Gly262=
ENST00000696083.1:n.1668A= (ADA)
ENST00000696084.1:n.888A= (ADA)
ENST00000696104.1:c.395A= (ADA) ENSP00000512399.1:p.Asp132=
ENST00000372874.9:c.711A= (ADA) MANE Select ENSP00000361965.4:p.Gly237=
ENST00000372874.8:c.711A= (ADA) ENSP00000361965.4:p.Gly237=
ENST00000372887.5:c.152-1035T= (PKIG) ENSP00000361978.1:n.152-1035T=
ENST00000464097.5:n.461A= (ADA)
ENST00000492931.5:n.871A= (ADA)
ENST00000536532.5:c.711A= (ADA) ENSP00000440946.1:p.Gly237=
ENST00000537820.1:c.639A= (ADA) ENSP00000441818.1:p.Gly213=
ENST00000539235.5:c.*95A= (ADA) ENSP00000446464.1:n.*95A=
NM_000022.2:c.711A= , LRG_16t1:c.711A= (ADA) NP_000013.2:p.Gly237=
XM_005260236.2:c.639A= (ADA) XP_005260293.1:p.Gly213=
XM_011528478.1:c.306A= (ADA) XP_011526780.1:p.Gly102=
XM_011528479.1:c.306A= (ADA) XP_011526781.1:p.Gly102=
XR_244129.1:n.765A= (ADA)
NM_000022.3:c.711A= (ADA) NP_000013.2:p.Gly237=
NM_001322050.1:c.306A= (ADA) NP_001308979.1:p.Gly102=
NM_001322051.1:c.639A= (ADA) NP_001308980.1:p.Gly213=
NR_136160.1:n.862A= (ADA)
NM_000022.4:c.711A= (ADA) MANE Select NP_000013.2:p.Gly237=
NM_001322050.2:c.306A= (ADA) NP_001308979.1:p.Gly102=
NM_001322051.2:c.639A= (ADA) NP_001308980.1:p.Gly213=
NR_136160.2:n.803A= (ADA)