Canonical Allele Identifier: CA510591385

Linked Data

MyVariant Identifiers: chr20:g.43248950T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620309T>G , CM000682.2:g.44620309T>G GRCh38
NC_000020.10:g.43248950T>G , CM000682.1:g.43248950T>G GRCh37
NC_000020.9:g.42682364T>G NCBI36
NG_007385.1:g.36427A>C , LRG_16:g.36427A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.1235A>C (ADA)
ENST00000536076.2:c.915A>C (ADA) ENSP00000512234.1:p.Ser305=
ENST00000536532.6:c.*211A>C (ADA) ENSP00000440946.1:n.*211A>C
ENST00000537820.2:c.996A>C (ADA) ENSP00000441818.1:p.Ser332=
ENST00000539235.6:c.*452A>C (ADA) ENSP00000446464.1:n.*452A>C
ENST00000695889.1:c.543A>C (ADA) ENSP00000512240.1:p.Ser181=
ENST00000695890.1:n.5179A>C (ADA)
ENST00000695891.1:c.608A>C (ADA) ENSP00000512241.1:n.608A>C
ENST00000695927.1:c.1146A>C (ADA) ENSP00000512270.1:p.Ser382=
ENST00000695949.1:c.993A>C (ADA) ENSP00000512281.1:p.Ser331=
ENST00000695956.1:c.223A>C (ADA)
ENST00000695957.1:c.*559A>C (ADA) ENSP00000512286.1:n.*559A>C
ENST00000695991.1:c.606A>C (ADA) ENSP00000512314.1:p.Ser202=
ENST00000695992.1:c.*211A>C (ADA) ENSP00000512315.1:n.*211A>C
ENST00000695993.1:c.1068A>C (ADA) ENSP00000512316.1:p.Ser356=
ENST00000695994.1:c.*211A>C (ADA) ENSP00000512317.1:n.*211A>C
ENST00000695995.1:c.678A>C (ADA) ENSP00000512318.1:p.Ser226=
ENST00000695996.1:n.1150A>C (ADA)
ENST00000696003.1:n.2852A>C (ADA)
ENST00000696004.1:n.1852A>C (ADA)
ENST00000696005.1:c.518A>C (ADA)
ENST00000696006.1:c.*211A>C (ADA) ENSP00000512325.1:n.*211A>C
ENST00000696007.1:c.995A>C (ADA) ENSP00000512326.1:n.995A>C
ENST00000696008.1:n.3422A>C (ADA)
ENST00000696017.1:c.1065A>C (ADA) ENSP00000512333.1:p.Ser355=
ENST00000696034.1:c.*211A>C (ADA) ENSP00000512343.1:n.*211A>C
ENST00000696035.1:n.1254A>C (ADA)
ENST00000696036.1:n.1769A>C (ADA)
ENST00000696037.1:n.2745A>C (ADA)
ENST00000696038.1:c.*825A>C (ADA) ENSP00000512344.1:n.*825A>C
ENST00000696039.1:n.1432A>C (ADA)
ENST00000696058.1:c.1065A>C (ADA) ENSP00000512361.1:p.Ser355=
ENST00000696059.1:c.*1013A>C (ADA) ENSP00000512362.1:n.*1013A>C
ENST00000696060.1:c.1137A>C (ADA) ENSP00000512363.1:p.Ser379=
ENST00000696061.1:c.1065A>C (ADA) ENSP00000512364.1:p.Ser355=
ENST00000696062.1:c.1131A>C (ADA) ENSP00000512365.1:p.Ser377=
ENST00000696063.1:c.1143A>C (ADA) ENSP00000512366.1:p.Ser381=
ENST00000696064.1:c.915A>C (ADA) ENSP00000512367.1:p.Ser305=
ENST00000696065.1:c.390A>C (ADA) ENSP00000512368.1:p.Ser130=
ENST00000696072.1:n.423A>C (ADA)
ENST00000696073.1:n.1379A>C (ADA)
ENST00000696074.1:n.619A>C (ADA)
ENST00000696075.1:c.*1038A>C (ADA) ENSP00000512374.1:n.*1038A>C
ENST00000696076.1:c.1137A>C (ADA) ENSP00000512375.1:p.Ser379=
ENST00000696077.1:c.1062A>C (ADA) ENSP00000512376.1:p.Ser354=
ENST00000696078.1:c.1065A>C (ADA) ENSP00000512377.1:p.Ser355=
ENST00000696079.1:c.1065A>C (ADA) ENSP00000512378.1:p.Ser355=
ENST00000696080.1:c.1068A>C (ADA) ENSP00000512379.1:p.Ser356=
ENST00000696081.1:n.1187A>C (ADA)
ENST00000696082.1:c.1143A>C (ADA) ENSP00000512380.1:p.Ser381=
ENST00000696083.1:n.2025A>C (ADA)
ENST00000696084.1:n.1245A>C (ADA)
ENST00000696104.1:c.*137A>C (ADA) ENSP00000512399.1:n.*137A>C
ENST00000372874.9:c.1068A>C (ADA) MANE Select ENSP00000361965.4:p.Ser356=
ENST00000372874.8:c.1068A>C (ADA) ENSP00000361965.4:p.Ser356=
ENST00000372887.5:c.152-3624T>G (PKIG) ENSP00000361978.1:n.152-3624T>G
ENST00000464097.5:n.1434A>C (ADA)
ENST00000492931.5:n.1228A>C (ADA)
ENST00000536532.5:c.*211A>C (ADA) ENSP00000440946.1:n.*211A>C
ENST00000537820.1:c.996A>C (ADA) ENSP00000441818.1:p.Ser332=
ENST00000539235.5:c.*452A>C (ADA) ENSP00000446464.1:n.*452A>C
NM_000022.2:c.1068A>C , LRG_16t1:c.1068A>C (ADA) NP_000013.2:p.Ser356=
XM_005260236.2:c.996A>C (ADA) XP_005260293.1:p.Ser332=
XM_011528478.1:c.663A>C (ADA) XP_011526780.1:p.Ser221=
XM_011528479.1:c.663A>C (ADA) XP_011526781.1:p.Ser221=
XR_244129.1:n.1057A>C (ADA)
NM_000022.3:c.1068A>C (ADA) NP_000013.2:p.Ser356=
NM_001322050.1:c.663A>C (ADA) NP_001308979.1:p.Ser221=
NM_001322051.1:c.996A>C (ADA) NP_001308980.1:p.Ser332=
NR_136160.1:n.1154A>C (ADA)
NM_000022.4:c.1068A>C (ADA) MANE Select NP_000013.2:p.Ser356=
NM_001322050.2:c.663A>C (ADA) NP_001308979.1:p.Ser221=
NM_001322051.2:c.996A>C (ADA) NP_001308980.1:p.Ser332=
NR_136160.2:n.1095A>C (ADA)