Canonical Allele Identifier: CA409120891
Gene: ADA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624278A>G , CM000682.2:g.44624278A>G GRCh38
NC_000020.10:g.43252919A>G , CM000682.1:g.43252919A>G GRCh37
NC_000020.9:g.42686333A>G NCBI36
NG_007385.1:g.32458T>C , LRG_16:g.32458T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.621T>C
ENST00000536076.2:c.377T>C ENSP00000512234.1:p.Val126Ala
ENST00000536532.6:c.530T>C ENSP00000440946.1:p.Val177Ala
ENST00000537820.2:c.530T>C ENSP00000441818.1:p.Val177Ala
ENST00000539235.6:c.219-1200T>C ENSP00000446464.1:n.219-1200T>C
ENST00000695889.1:c.219-1348T>C ENSP00000512240.1:n.219-1348T>C
ENST00000695890.1:n.2333T>C
ENST00000695891.1:c.219-1348T>C ENSP00000512241.1:n.219-1348T>C
ENST00000695927.1:c.608T>C ENSP00000512270.1:p.Val203Ala
ENST00000695949.1:c.527T>C ENSP00000512281.1:p.Val176Ala
ENST00000695957.1:c.*21T>C ENSP00000512286.1:n.*21T>C
ENST00000695991.1:c.217-1348T>C ENSP00000512314.1:n.217-1348T>C
ENST00000695992.1:c.530T>C ENSP00000512315.1:p.Val177Ala
ENST00000695993.1:c.530T>C ENSP00000512316.1:p.Val177Ala
ENST00000695994.1:c.530T>C ENSP00000512317.1:p.Val177Ala
ENST00000695995.1:c.217-1200T>C ENSP00000512318.1:n.217-1200T>C
ENST00000695996.1:n.601T>C
ENST00000695997.1:n.485T>C
ENST00000696003.1:n.622T>C
ENST00000696004.1:n.622T>C
ENST00000696005.1:c.52T>C
ENST00000696006.1:c.530T>C ENSP00000512325.1:p.Val177Ala
ENST00000696007.1:c.381T>C ENSP00000512326.1:n.381T>C
ENST00000696008.1:n.1685T>C
ENST00000696009.1:n.1880T>C
ENST00000696017.1:c.527T>C ENSP00000512333.1:p.Val176Ala
ENST00000696034.1:c.530T>C ENSP00000512343.1:p.Val177Ala
ENST00000696035.1:n.640T>C
ENST00000696036.1:n.1220T>C
ENST00000696037.1:n.2207T>C
ENST00000696038.1:c.*276T>C ENSP00000512344.1:n.*276T>C
ENST00000696039.1:n.818T>C
ENST00000696058.1:c.530T>C ENSP00000512361.1:p.Val177Ala
ENST00000696059.1:c.*475T>C ENSP00000512362.1:n.*475T>C
ENST00000696060.1:c.530T>C ENSP00000512363.1:p.Val177Ala
ENST00000696061.1:c.527T>C ENSP00000512364.1:p.Val176Ala
ENST00000696062.1:c.593T>C ENSP00000512365.1:p.Val198Ala
ENST00000696063.1:c.605T>C ENSP00000512366.1:p.Val202Ala
ENST00000696064.1:c.377T>C ENSP00000512367.1:p.Val126Ala
ENST00000696065.1:c.66-1348T>C ENSP00000512368.1:n.66-1348T>C
ENST00000696074.1:n.146T>C
ENST00000696075.1:c.*500T>C ENSP00000512374.1:n.*500T>C
ENST00000696076.1:c.530T>C ENSP00000512375.1:p.Val177Ala
ENST00000696077.1:c.527T>C ENSP00000512376.1:p.Val176Ala
ENST00000696078.1:c.530T>C ENSP00000512377.1:p.Val177Ala
ENST00000696079.1:c.530T>C ENSP00000512378.1:p.Val177Ala
ENST00000696080.1:c.530T>C ENSP00000512379.1:p.Val177Ala
ENST00000696081.1:n.649T>C
ENST00000696082.1:c.608T>C ENSP00000512380.1:p.Val203Ala
ENST00000696083.1:n.1411T>C
ENST00000696084.1:n.631T>C
ENST00000696104.1:c.363-1348T>C ENSP00000512399.1:n.363-1348T>C
ENST00000696105.1:c.*71T>C ENSP00000512400.1:n.*71T>C
ENST00000372874.9:c.530T>C MANE Select ENSP00000361965.4:p.Val177Ala
ENST00000372874.8:c.530T>C ENSP00000361965.4:p.Val177Ala
ENST00000464097.5:n.204T>C
ENST00000492931.5:n.614T>C
ENST00000536532.5:c.530T>C ENSP00000440946.1:p.Val177Ala
ENST00000537820.1:c.530T>C ENSP00000441818.1:p.Val177Ala
ENST00000539235.5:c.219-1200T>C ENSP00000446464.1:n.219-1200T>C
NM_000022.2:c.530T>C , LRG_16t1:c.530T>C NP_000013.2:p.Val177Ala
XM_005260236.2:c.530T>C XP_005260293.1:p.Val177Ala
XM_011528478.1:c.125T>C XP_011526780.1:p.Val42Ala
XM_011528479.1:c.125T>C XP_011526781.1:p.Val42Ala
XR_244129.1:n.584T>C
NM_000022.3:c.530T>C NP_000013.2:p.Val177Ala
NM_001322050.1:c.125T>C NP_001308979.1:p.Val42Ala
NM_001322051.1:c.530T>C NP_001308980.1:p.Val177Ala
NR_136160.1:n.681T>C
NM_000022.4:c.530T>C MANE Select NP_000013.2:p.Val177Ala
NM_001322050.2:c.125T>C NP_001308979.1:p.Val42Ala
NM_001322051.2:c.530T>C NP_001308980.1:p.Val177Ala
NR_136160.2:n.622T>C