Canonical Allele Identifier: CA409120515

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623077T>A , CM000682.2:g.44623077T>A GRCh38
NC_000020.10:g.43251718T>A , CM000682.1:g.43251718T>A GRCh37
NC_000020.9:g.42685132T>A NCBI36
NG_007385.1:g.33659A>T , LRG_16:g.33659A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.699A>T (ADA)
ENST00000536076.2:c.455A>T (ADA) ENSP00000512234.1:p.Glu152Val
ENST00000536532.6:c.608A>T (ADA) ENSP00000440946.1:p.Glu203Val
ENST00000537820.2:c.607-147A>T (ADA) ENSP00000441818.1:n.607-147A>T
ENST00000539235.6:c.220A>T (ADA) ENSP00000446464.1:p.Arg74Trp
ENST00000695889.1:c.219-147A>T (ADA) ENSP00000512240.1:n.219-147A>T
ENST00000695890.1:n.2411A>T (ADA)
ENST00000695891.1:c.219-147A>T (ADA) ENSP00000512241.1:n.219-147A>T
ENST00000695927.1:c.686A>T (ADA) ENSP00000512270.1:p.Glu229Val
ENST00000695949.1:c.604-147A>T (ADA) ENSP00000512281.1:n.604-147A>T
ENST00000695957.1:c.*99A>T (ADA) ENSP00000512286.1:n.*99A>T
ENST00000695991.1:c.217-147A>T (ADA) ENSP00000512314.1:n.217-147A>T
ENST00000695992.1:c.608A>T (ADA) ENSP00000512315.1:p.Glu203Val
ENST00000695993.1:c.608A>T (ADA) ENSP00000512316.1:p.Glu203Val
ENST00000695994.1:c.608A>T (ADA) ENSP00000512317.1:p.Glu203Val
ENST00000695995.1:c.218A>T (ADA) ENSP00000512318.1:p.Glu73Val
ENST00000695996.1:n.679A>T (ADA)
ENST00000696003.1:n.700A>T (ADA)
ENST00000696004.1:n.700A>T (ADA)
ENST00000696005.1:c.129-147A>T (ADA)
ENST00000696006.1:c.607-147A>T (ADA) ENSP00000512325.1:n.607-147A>T
ENST00000696007.1:c.459A>T (ADA) ENSP00000512326.1:n.459A>T
ENST00000696008.1:n.2886A>T (ADA)
ENST00000696017.1:c.605A>T (ADA) ENSP00000512333.1:p.Glu202Val
ENST00000696034.1:c.608A>T (ADA) ENSP00000512343.1:p.Glu203Val
ENST00000696035.1:n.718A>T (ADA)
ENST00000696036.1:n.1298A>T (ADA)
ENST00000696037.1:n.2285A>T (ADA)
ENST00000696038.1:c.*354A>T (ADA) ENSP00000512344.1:n.*354A>T
ENST00000696039.1:n.896A>T (ADA)
ENST00000696058.1:c.607-2A>T (ADA) ENSP00000512361.1:n.607-2A>T
ENST00000696059.1:c.*553A>T (ADA) ENSP00000512362.1:n.*553A>T
ENST00000696060.1:c.677A>T (ADA) ENSP00000512363.1:p.Glu226Val
ENST00000696061.1:c.605A>T (ADA) ENSP00000512364.1:p.Glu202Val
ENST00000696062.1:c.671A>T (ADA) ENSP00000512365.1:p.Glu224Val
ENST00000696063.1:c.683A>T (ADA) ENSP00000512366.1:p.Glu228Val
ENST00000696064.1:c.455A>T (ADA) ENSP00000512367.1:p.Glu152Val
ENST00000696065.1:c.66-147A>T (ADA) ENSP00000512368.1:n.66-147A>T
ENST00000696073.1:n.843A>T (ADA)
ENST00000696074.1:n.224A>T (ADA)
ENST00000696075.1:c.*578A>T (ADA) ENSP00000512374.1:n.*578A>T
ENST00000696076.1:c.677A>T (ADA) ENSP00000512375.1:p.Glu226Val
ENST00000696077.1:c.604-2A>T (ADA) ENSP00000512376.1:n.604-2A>T
ENST00000696078.1:c.607-2A>T (ADA) ENSP00000512377.1:n.607-2A>T
ENST00000696079.1:c.607-2A>T (ADA) ENSP00000512378.1:n.607-2A>T
ENST00000696080.1:c.608A>T (ADA) ENSP00000512379.1:p.Glu203Val
ENST00000696081.1:n.727A>T (ADA)
ENST00000696082.1:c.685-2A>T (ADA) ENSP00000512380.1:n.685-2A>T
ENST00000696083.1:n.1489A>T (ADA)
ENST00000696084.1:n.709A>T (ADA)
ENST00000696104.1:c.363-147A>T (ADA) ENSP00000512399.1:n.363-147A>T
ENST00000696105.1:c.*149A>T (ADA) ENSP00000512400.1:n.*149A>T
ENST00000372874.9:c.608A>T (ADA) MANE Select ENSP00000361965.4:p.Glu203Val
ENST00000372874.8:c.608A>T (ADA) ENSP00000361965.4:p.Glu203Val
ENST00000372887.5:c.152-856T>A (PKIG) ENSP00000361978.1:n.152-856T>A
ENST00000464097.5:n.282A>T (ADA)
ENST00000492931.5:n.692A>T (ADA)
ENST00000536532.5:c.608A>T (ADA) ENSP00000440946.1:p.Glu203Val
ENST00000537820.1:c.607-147A>T (ADA) ENSP00000441818.1:n.607-147A>T
ENST00000539235.5:c.220A>T (ADA) ENSP00000446464.1:p.Arg74Trp
NM_000022.2:c.608A>T , LRG_16t1:c.608A>T (ADA) NP_000013.2:p.Glu203Val
XM_005260236.2:c.607-147A>T (ADA) XP_005260293.1:n.607-147A>T
XM_011528478.1:c.203A>T (ADA) XP_011526780.1:p.Glu68Val
XM_011528479.1:c.203A>T (ADA) XP_011526781.1:p.Glu68Val
XR_244129.1:n.662A>T (ADA)
NM_000022.3:c.608A>T (ADA) NP_000013.2:p.Glu203Val
NM_001322050.1:c.203A>T (ADA) NP_001308979.1:p.Glu68Val
NM_001322051.1:c.607-147A>T (ADA) NP_001308980.1:n.607-147A>T
NR_136160.1:n.759A>T (ADA)
NM_000022.4:c.608A>T (ADA) MANE Select NP_000013.2:p.Glu203Val
NM_001322050.2:c.203A>T (ADA) NP_001308979.1:p.Glu68Val
NM_001322051.2:c.607-147A>T (ADA) NP_001308980.1:n.607-147A>T
NR_136160.2:n.700A>T (ADA)