Canonical Allele Identifier: CA510591831

Linked Data

MyVariant Identifiers: chr20:g.43248980C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620339C>G , CM000682.2:g.44620339C>G GRCh38
NC_000020.10:g.43248980C>G , CM000682.1:g.43248980C>G GRCh37
NC_000020.9:g.42682394C>G NCBI36
NG_007385.1:g.36397G>C , LRG_16:g.36397G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.1205G>C (ADA)
ENST00000536076.2:c.885G>C (ADA) ENSP00000512234.1:p.Leu295=
ENST00000536532.6:c.*181G>C (ADA) ENSP00000440946.1:n.*181G>C
ENST00000537820.2:c.966G>C (ADA) ENSP00000441818.1:p.Leu322=
ENST00000539235.6:c.*422G>C (ADA) ENSP00000446464.1:n.*422G>C
ENST00000695889.1:c.513G>C (ADA) ENSP00000512240.1:p.Leu171=
ENST00000695890.1:n.5149G>C (ADA)
ENST00000695891.1:c.578G>C (ADA) ENSP00000512241.1:n.578G>C
ENST00000695927.1:c.1116G>C (ADA) ENSP00000512270.1:p.Leu372=
ENST00000695949.1:c.963G>C (ADA) ENSP00000512281.1:p.Leu321=
ENST00000695956.1:c.193G>C (ADA)
ENST00000695957.1:c.*529G>C (ADA) ENSP00000512286.1:n.*529G>C
ENST00000695991.1:c.576G>C (ADA) ENSP00000512314.1:p.Leu192=
ENST00000695992.1:c.*181G>C (ADA) ENSP00000512315.1:n.*181G>C
ENST00000695993.1:c.1038G>C (ADA) ENSP00000512316.1:p.Leu346=
ENST00000695994.1:c.*181G>C (ADA) ENSP00000512317.1:n.*181G>C
ENST00000695995.1:c.648G>C (ADA) ENSP00000512318.1:p.Leu216=
ENST00000695996.1:n.1120G>C (ADA)
ENST00000696003.1:n.2822G>C (ADA)
ENST00000696004.1:n.1822G>C (ADA)
ENST00000696005.1:c.488G>C (ADA)
ENST00000696006.1:c.*181G>C (ADA) ENSP00000512325.1:n.*181G>C
ENST00000696007.1:c.965G>C (ADA) ENSP00000512326.1:n.965G>C
ENST00000696008.1:n.3392G>C (ADA)
ENST00000696017.1:c.1035G>C (ADA) ENSP00000512333.1:p.Leu345=
ENST00000696034.1:c.*181G>C (ADA) ENSP00000512343.1:n.*181G>C
ENST00000696035.1:n.1224G>C (ADA)
ENST00000696036.1:n.1739G>C (ADA)
ENST00000696037.1:n.2715G>C (ADA)
ENST00000696038.1:c.*795G>C (ADA) ENSP00000512344.1:n.*795G>C
ENST00000696039.1:n.1402G>C (ADA)
ENST00000696058.1:c.1035G>C (ADA) ENSP00000512361.1:p.Leu345=
ENST00000696059.1:c.*983G>C (ADA) ENSP00000512362.1:n.*983G>C
ENST00000696060.1:c.1107G>C (ADA) ENSP00000512363.1:p.Leu369=
ENST00000696061.1:c.1035G>C (ADA) ENSP00000512364.1:p.Leu345=
ENST00000696062.1:c.1101G>C (ADA) ENSP00000512365.1:p.Leu367=
ENST00000696063.1:c.1113G>C (ADA) ENSP00000512366.1:p.Leu371=
ENST00000696064.1:c.885G>C (ADA) ENSP00000512367.1:p.Leu295=
ENST00000696065.1:c.360G>C (ADA) ENSP00000512368.1:p.Leu120=
ENST00000696072.1:n.393G>C (ADA)
ENST00000696073.1:n.1349G>C (ADA)
ENST00000696074.1:n.589G>C (ADA)
ENST00000696075.1:c.*1008G>C (ADA) ENSP00000512374.1:n.*1008G>C
ENST00000696076.1:c.1107G>C (ADA) ENSP00000512375.1:p.Leu369=
ENST00000696077.1:c.1032G>C (ADA) ENSP00000512376.1:p.Leu344=
ENST00000696078.1:c.1035G>C (ADA) ENSP00000512377.1:p.Leu345=
ENST00000696079.1:c.1035G>C (ADA) ENSP00000512378.1:p.Leu345=
ENST00000696080.1:c.1038G>C (ADA) ENSP00000512379.1:p.Leu346=
ENST00000696081.1:n.1157G>C (ADA)
ENST00000696082.1:c.1113G>C (ADA) ENSP00000512380.1:p.Leu371=
ENST00000696083.1:n.1995G>C (ADA)
ENST00000696084.1:n.1215G>C (ADA)
ENST00000696104.1:c.*107G>C (ADA) ENSP00000512399.1:n.*107G>C
ENST00000372874.9:c.1038G>C (ADA) MANE Select ENSP00000361965.4:p.Leu346=
ENST00000372874.8:c.1038G>C (ADA) ENSP00000361965.4:p.Leu346=
ENST00000372887.5:c.152-3594C>G (PKIG) ENSP00000361978.1:n.152-3594C>G
ENST00000464097.5:n.1404G>C (ADA)
ENST00000492931.5:n.1198G>C (ADA)
ENST00000536532.5:c.*181G>C (ADA) ENSP00000440946.1:n.*181G>C
ENST00000537820.1:c.966G>C (ADA) ENSP00000441818.1:p.Leu322=
ENST00000539235.5:c.*422G>C (ADA) ENSP00000446464.1:n.*422G>C
NM_000022.2:c.1038G>C , LRG_16t1:c.1038G>C (ADA) NP_000013.2:p.Leu346=
XM_005260236.2:c.966G>C (ADA) XP_005260293.1:p.Leu322=
XM_011528478.1:c.633G>C (ADA) XP_011526780.1:p.Leu211=
XM_011528479.1:c.633G>C (ADA) XP_011526781.1:p.Leu211=
XR_244129.1:n.1027G>C (ADA)
NM_000022.3:c.1038G>C (ADA) NP_000013.2:p.Leu346=
NM_001322050.1:c.633G>C (ADA) NP_001308979.1:p.Leu211=
NM_001322051.1:c.966G>C (ADA) NP_001308980.1:p.Leu322=
NR_136160.1:n.1124G>C (ADA)
NM_000022.4:c.1038G>C (ADA) MANE Select NP_000013.2:p.Leu346=
NM_001322050.2:c.633G>C (ADA) NP_001308979.1:p.Leu211=
NM_001322051.2:c.966G>C (ADA) NP_001308980.1:p.Leu322=
NR_136160.2:n.1065G>C (ADA)