Canonical Allele Identifier: CA409118644

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620380T>A , CM000682.2:g.44620380T>A GRCh38
NC_000020.10:g.43249021T>A , CM000682.1:g.43249021T>A GRCh37
NC_000020.9:g.42682435T>A NCBI36
NG_007385.1:g.36356A>T , LRG_16:g.36356A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.1164A>T (ADA)
ENST00000536076.2:c.844A>T (ADA) ENSP00000512234.1:p.Ser282Cys
ENST00000536532.6:c.*140A>T (ADA) ENSP00000440946.1:n.*140A>T
ENST00000537820.2:c.925A>T (ADA) ENSP00000441818.1:p.Ser309Cys
ENST00000539235.6:c.*381A>T (ADA) ENSP00000446464.1:n.*381A>T
ENST00000695889.1:c.472A>T (ADA) ENSP00000512240.1:p.Ser158Cys
ENST00000695890.1:n.5108A>T (ADA)
ENST00000695891.1:c.537A>T (ADA) ENSP00000512241.1:n.537A>T
ENST00000695927.1:c.1075A>T (ADA) ENSP00000512270.1:p.Ser359Cys
ENST00000695949.1:c.922A>T (ADA) ENSP00000512281.1:p.Ser308Cys
ENST00000695956.1:c.152A>T (ADA)
ENST00000695957.1:c.*488A>T (ADA) ENSP00000512286.1:n.*488A>T
ENST00000695991.1:c.535A>T (ADA) ENSP00000512314.1:p.Ser179Cys
ENST00000695992.1:c.*140A>T (ADA) ENSP00000512315.1:n.*140A>T
ENST00000695993.1:c.997A>T (ADA) ENSP00000512316.1:p.Ser333Cys
ENST00000695994.1:c.*140A>T (ADA) ENSP00000512317.1:n.*140A>T
ENST00000695995.1:c.607A>T (ADA) ENSP00000512318.1:p.Ser203Cys
ENST00000695996.1:n.1079A>T (ADA)
ENST00000696003.1:n.2781A>T (ADA)
ENST00000696004.1:n.1781A>T (ADA)
ENST00000696005.1:c.447A>T (ADA)
ENST00000696006.1:c.*140A>T (ADA) ENSP00000512325.1:n.*140A>T
ENST00000696007.1:c.924A>T (ADA) ENSP00000512326.1:n.924A>T
ENST00000696008.1:n.3351A>T (ADA)
ENST00000696017.1:c.994A>T (ADA) ENSP00000512333.1:p.Ser332Cys
ENST00000696034.1:c.*140A>T (ADA) ENSP00000512343.1:n.*140A>T
ENST00000696035.1:n.1183A>T (ADA)
ENST00000696036.1:n.1698A>T (ADA)
ENST00000696037.1:n.2674A>T (ADA)
ENST00000696038.1:c.*754A>T (ADA) ENSP00000512344.1:n.*754A>T
ENST00000696039.1:n.1361A>T (ADA)
ENST00000696058.1:c.994A>T (ADA) ENSP00000512361.1:p.Ser332Cys
ENST00000696059.1:c.*942A>T (ADA) ENSP00000512362.1:n.*942A>T
ENST00000696060.1:c.1066A>T (ADA) ENSP00000512363.1:p.Ser356Cys
ENST00000696061.1:c.994A>T (ADA) ENSP00000512364.1:p.Ser332Cys
ENST00000696062.1:c.1060A>T (ADA) ENSP00000512365.1:p.Ser354Cys
ENST00000696063.1:c.1072A>T (ADA) ENSP00000512366.1:p.Ser358Cys
ENST00000696064.1:c.844A>T (ADA) ENSP00000512367.1:p.Ser282Cys
ENST00000696065.1:c.319A>T (ADA) ENSP00000512368.1:p.Ser107Cys
ENST00000696072.1:n.352A>T (ADA)
ENST00000696073.1:n.1308A>T (ADA)
ENST00000696074.1:n.548A>T (ADA)
ENST00000696075.1:c.*967A>T (ADA) ENSP00000512374.1:n.*967A>T
ENST00000696076.1:c.1066A>T (ADA) ENSP00000512375.1:p.Ser356Cys
ENST00000696077.1:c.991A>T (ADA) ENSP00000512376.1:p.Ser331Cys
ENST00000696078.1:c.994A>T (ADA) ENSP00000512377.1:p.Ser332Cys
ENST00000696079.1:c.994A>T (ADA) ENSP00000512378.1:p.Ser332Cys
ENST00000696080.1:c.997A>T (ADA) ENSP00000512379.1:p.Ser333Cys
ENST00000696081.1:n.1116A>T (ADA)
ENST00000696082.1:c.1072A>T (ADA) ENSP00000512380.1:p.Ser358Cys
ENST00000696083.1:n.1954A>T (ADA)
ENST00000696084.1:n.1174A>T (ADA)
ENST00000696104.1:c.*66A>T (ADA) ENSP00000512399.1:n.*66A>T
ENST00000372874.9:c.997A>T (ADA) MANE Select ENSP00000361965.4:p.Ser333Cys
ENST00000372874.8:c.997A>T (ADA) ENSP00000361965.4:p.Ser333Cys
ENST00000372887.5:c.152-3553T>A (PKIG) ENSP00000361978.1:n.152-3553T>A
ENST00000464097.5:n.1363A>T (ADA)
ENST00000492931.5:n.1157A>T (ADA)
ENST00000536532.5:c.*140A>T (ADA) ENSP00000440946.1:n.*140A>T
ENST00000537820.1:c.925A>T (ADA) ENSP00000441818.1:p.Ser309Cys
ENST00000539235.5:c.*381A>T (ADA) ENSP00000446464.1:n.*381A>T
NM_000022.2:c.997A>T , LRG_16t1:c.997A>T (ADA) NP_000013.2:p.Ser333Cys
XM_005260236.2:c.925A>T (ADA) XP_005260293.1:p.Ser309Cys
XM_011528478.1:c.592A>T (ADA) XP_011526780.1:p.Ser198Cys
XM_011528479.1:c.592A>T (ADA) XP_011526781.1:p.Ser198Cys
XR_244129.1:n.986A>T (ADA)
NM_000022.3:c.997A>T (ADA) NP_000013.2:p.Ser333Cys
NM_001322050.1:c.592A>T (ADA) NP_001308979.1:p.Ser198Cys
NM_001322051.1:c.925A>T (ADA) NP_001308980.1:p.Ser309Cys
NR_136160.1:n.1083A>T (ADA)
NM_000022.4:c.997A>T (ADA) MANE Select NP_000013.2:p.Ser333Cys
NM_001322050.2:c.592A>T (ADA) NP_001308979.1:p.Ser198Cys
NM_001322051.2:c.925A>T (ADA) NP_001308980.1:p.Ser309Cys
NR_136160.2:n.1024A>T (ADA)