Canonical Allele Identifier: CA409118595

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620359T>A , CM000682.2:g.44620359T>A GRCh38
NC_000020.10:g.43249000T>A , CM000682.1:g.43249000T>A GRCh37
NC_000020.9:g.42682414T>A NCBI36
NG_007385.1:g.36377A>T , LRG_16:g.36377A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.1185A>T (ADA)
ENST00000536076.2:c.865A>T (ADA) ENSP00000512234.1:p.Lys289Ter
ENST00000536532.6:c.*161A>T (ADA) ENSP00000440946.1:n.*161A>T
ENST00000537820.2:c.946A>T (ADA) ENSP00000441818.1:p.Lys316Ter
ENST00000539235.6:c.*402A>T (ADA) ENSP00000446464.1:n.*402A>T
ENST00000695889.1:c.493A>T (ADA) ENSP00000512240.1:p.Lys165Ter
ENST00000695890.1:n.5129A>T (ADA)
ENST00000695891.1:c.558A>T (ADA) ENSP00000512241.1:n.558A>T
ENST00000695927.1:c.1096A>T (ADA) ENSP00000512270.1:p.Lys366Ter
ENST00000695949.1:c.943A>T (ADA) ENSP00000512281.1:p.Lys315Ter
ENST00000695956.1:c.173A>T (ADA)
ENST00000695957.1:c.*509A>T (ADA) ENSP00000512286.1:n.*509A>T
ENST00000695991.1:c.556A>T (ADA) ENSP00000512314.1:p.Lys186Ter
ENST00000695992.1:c.*161A>T (ADA) ENSP00000512315.1:n.*161A>T
ENST00000695993.1:c.1018A>T (ADA) ENSP00000512316.1:p.Lys340Ter
ENST00000695994.1:c.*161A>T (ADA) ENSP00000512317.1:n.*161A>T
ENST00000695995.1:c.628A>T (ADA) ENSP00000512318.1:p.Lys210Ter
ENST00000695996.1:n.1100A>T (ADA)
ENST00000696003.1:n.2802A>T (ADA)
ENST00000696004.1:n.1802A>T (ADA)
ENST00000696005.1:c.468A>T (ADA)
ENST00000696006.1:c.*161A>T (ADA) ENSP00000512325.1:n.*161A>T
ENST00000696007.1:c.945A>T (ADA) ENSP00000512326.1:n.945A>T
ENST00000696008.1:n.3372A>T (ADA)
ENST00000696017.1:c.1015A>T (ADA) ENSP00000512333.1:p.Lys339Ter
ENST00000696034.1:c.*161A>T (ADA) ENSP00000512343.1:n.*161A>T
ENST00000696035.1:n.1204A>T (ADA)
ENST00000696036.1:n.1719A>T (ADA)
ENST00000696037.1:n.2695A>T (ADA)
ENST00000696038.1:c.*775A>T (ADA) ENSP00000512344.1:n.*775A>T
ENST00000696039.1:n.1382A>T (ADA)
ENST00000696058.1:c.1015A>T (ADA) ENSP00000512361.1:p.Lys339Ter
ENST00000696059.1:c.*963A>T (ADA) ENSP00000512362.1:n.*963A>T
ENST00000696060.1:c.1087A>T (ADA) ENSP00000512363.1:p.Lys363Ter
ENST00000696061.1:c.1015A>T (ADA) ENSP00000512364.1:p.Lys339Ter
ENST00000696062.1:c.1081A>T (ADA) ENSP00000512365.1:p.Lys361Ter
ENST00000696063.1:c.1093A>T (ADA) ENSP00000512366.1:p.Lys365Ter
ENST00000696064.1:c.865A>T (ADA) ENSP00000512367.1:p.Lys289Ter
ENST00000696065.1:c.340A>T (ADA) ENSP00000512368.1:p.Lys114Ter
ENST00000696072.1:n.373A>T (ADA)
ENST00000696073.1:n.1329A>T (ADA)
ENST00000696074.1:n.569A>T (ADA)
ENST00000696075.1:c.*988A>T (ADA) ENSP00000512374.1:n.*988A>T
ENST00000696076.1:c.1087A>T (ADA) ENSP00000512375.1:p.Lys363Ter
ENST00000696077.1:c.1012A>T (ADA) ENSP00000512376.1:p.Lys338Ter
ENST00000696078.1:c.1015A>T (ADA) ENSP00000512377.1:p.Lys339Ter
ENST00000696079.1:c.1015A>T (ADA) ENSP00000512378.1:p.Lys339Ter
ENST00000696080.1:c.1018A>T (ADA) ENSP00000512379.1:p.Lys340Ter
ENST00000696081.1:n.1137A>T (ADA)
ENST00000696082.1:c.1093A>T (ADA) ENSP00000512380.1:p.Lys365Ter
ENST00000696083.1:n.1975A>T (ADA)
ENST00000696084.1:n.1195A>T (ADA)
ENST00000696104.1:c.*87A>T (ADA) ENSP00000512399.1:n.*87A>T
ENST00000372874.9:c.1018A>T (ADA) MANE Select ENSP00000361965.4:p.Lys340Ter
ENST00000372874.8:c.1018A>T (ADA) ENSP00000361965.4:p.Lys340Ter
ENST00000372887.5:c.152-3574T>A (PKIG) ENSP00000361978.1:n.152-3574T>A
ENST00000464097.5:n.1384A>T (ADA)
ENST00000492931.5:n.1178A>T (ADA)
ENST00000536532.5:c.*161A>T (ADA) ENSP00000440946.1:n.*161A>T
ENST00000537820.1:c.946A>T (ADA) ENSP00000441818.1:p.Lys316Ter
ENST00000539235.5:c.*402A>T (ADA) ENSP00000446464.1:n.*402A>T
NM_000022.2:c.1018A>T , LRG_16t1:c.1018A>T (ADA) NP_000013.2:p.Lys340Ter
XM_005260236.2:c.946A>T (ADA) XP_005260293.1:p.Lys316Ter
XM_011528478.1:c.613A>T (ADA) XP_011526780.1:p.Lys205Ter
XM_011528479.1:c.613A>T (ADA) XP_011526781.1:p.Lys205Ter
XR_244129.1:n.1007A>T (ADA)
NM_000022.3:c.1018A>T (ADA) NP_000013.2:p.Lys340Ter
NM_001322050.1:c.613A>T (ADA) NP_001308979.1:p.Lys205Ter
NM_001322051.1:c.946A>T (ADA) NP_001308980.1:p.Lys316Ter
NR_136160.1:n.1104A>T (ADA)
NM_000022.4:c.1018A>T (ADA) MANE Select NP_000013.2:p.Lys340Ter
NM_001322050.2:c.613A>T (ADA) NP_001308979.1:p.Lys205Ter
NM_001322051.2:c.946A>T (ADA) NP_001308980.1:p.Lys316Ter
NR_136160.2:n.1045A>T (ADA)