Canonical Allele Identifier: CA409120993
Gene: ADA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624324A>G , CM000682.2:g.44624324A>G GRCh38
NC_000020.10:g.43252965A>G , CM000682.1:g.43252965A>G GRCh37
NC_000020.9:g.42686379A>G NCBI36
NG_007385.1:g.32412T>C , LRG_16:g.32412T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.575T>C
ENST00000536076.2:c.331T>C ENSP00000512234.1:p.Ser111Pro
ENST00000536532.6:c.484T>C ENSP00000440946.1:p.Ser162Pro
ENST00000537820.2:c.484T>C ENSP00000441818.1:p.Ser162Pro
ENST00000539235.6:c.219-1246T>C ENSP00000446464.1:n.219-1246T>C
ENST00000695889.1:c.219-1394T>C ENSP00000512240.1:n.219-1394T>C
ENST00000695890.1:n.2287T>C
ENST00000695891.1:c.219-1394T>C ENSP00000512241.1:n.219-1394T>C
ENST00000695927.1:c.562T>C ENSP00000512270.1:p.Ser188Pro
ENST00000695949.1:c.481T>C ENSP00000512281.1:p.Ser161Pro
ENST00000695957.1:c.368T>C ENSP00000512286.1:p.Val123Ala
ENST00000695991.1:c.217-1394T>C ENSP00000512314.1:n.217-1394T>C
ENST00000695992.1:c.484T>C ENSP00000512315.1:p.Ser162Pro
ENST00000695993.1:c.484T>C ENSP00000512316.1:p.Ser162Pro
ENST00000695994.1:c.484T>C ENSP00000512317.1:p.Ser162Pro
ENST00000695995.1:c.217-1246T>C ENSP00000512318.1:n.217-1246T>C
ENST00000695996.1:n.555T>C
ENST00000695997.1:n.439T>C
ENST00000696003.1:n.576T>C
ENST00000696004.1:n.576T>C
ENST00000696005.1:c.6T>C
ENST00000696006.1:c.484T>C ENSP00000512325.1:p.Ser162Pro
ENST00000696007.1:c.335T>C ENSP00000512326.1:p.Val112Ala
ENST00000696008.1:n.1639T>C
ENST00000696009.1:n.1834T>C
ENST00000696017.1:c.481T>C ENSP00000512333.1:p.Ser161Pro
ENST00000696034.1:c.484T>C ENSP00000512343.1:p.Ser162Pro
ENST00000696035.1:n.594T>C
ENST00000696036.1:n.1174T>C
ENST00000696037.1:n.2161T>C
ENST00000696038.1:c.*230T>C ENSP00000512344.1:n.*230T>C
ENST00000696039.1:n.772T>C
ENST00000696058.1:c.484T>C ENSP00000512361.1:p.Ser162Pro
ENST00000696059.1:c.*429T>C ENSP00000512362.1:n.*429T>C
ENST00000696060.1:c.484T>C ENSP00000512363.1:p.Ser162Pro
ENST00000696061.1:c.481T>C ENSP00000512364.1:p.Ser161Pro
ENST00000696062.1:c.547T>C ENSP00000512365.1:p.Ser183Pro
ENST00000696063.1:c.559T>C ENSP00000512366.1:p.Ser187Pro
ENST00000696064.1:c.331T>C ENSP00000512367.1:p.Ser111Pro
ENST00000696065.1:c.66-1394T>C ENSP00000512368.1:n.66-1394T>C
ENST00000696074.1:n.100T>C
ENST00000696075.1:c.*454T>C ENSP00000512374.1:n.*454T>C
ENST00000696076.1:c.484T>C ENSP00000512375.1:p.Ser162Pro
ENST00000696077.1:c.481T>C ENSP00000512376.1:p.Ser161Pro
ENST00000696078.1:c.484T>C ENSP00000512377.1:p.Ser162Pro
ENST00000696079.1:c.484T>C ENSP00000512378.1:p.Ser162Pro
ENST00000696080.1:c.484T>C ENSP00000512379.1:p.Ser162Pro
ENST00000696081.1:n.603T>C
ENST00000696082.1:c.562T>C ENSP00000512380.1:p.Ser188Pro
ENST00000696083.1:n.1365T>C
ENST00000696084.1:n.585T>C
ENST00000696104.1:c.363-1394T>C ENSP00000512399.1:n.363-1394T>C
ENST00000696105.1:c.*25T>C ENSP00000512400.1:n.*25T>C
ENST00000372874.9:c.484T>C MANE Select ENSP00000361965.4:p.Ser162Pro
ENST00000372874.8:c.484T>C ENSP00000361965.4:p.Ser162Pro
ENST00000464097.5:n.158T>C
ENST00000492931.5:n.568T>C
ENST00000536532.5:c.484T>C ENSP00000440946.1:p.Ser162Pro
ENST00000537820.1:c.484T>C ENSP00000441818.1:p.Ser162Pro
ENST00000539235.5:c.219-1246T>C ENSP00000446464.1:n.219-1246T>C
NM_000022.2:c.484T>C , LRG_16t1:c.484T>C NP_000013.2:p.Ser162Pro
XM_005260236.2:c.484T>C XP_005260293.1:p.Ser162Pro
XM_011528478.1:c.79T>C XP_011526780.1:p.Ser27Pro
XM_011528479.1:c.79T>C XP_011526781.1:p.Ser27Pro
XR_244129.1:n.538T>C
NM_000022.3:c.484T>C NP_000013.2:p.Ser162Pro
NM_001322050.1:c.79T>C NP_001308979.1:p.Ser27Pro
NM_001322051.1:c.484T>C NP_001308980.1:p.Ser162Pro
NR_136160.1:n.635T>C
NM_000022.4:c.484T>C MANE Select NP_000013.2:p.Ser162Pro
NM_001322050.2:c.79T>C NP_001308979.1:p.Ser27Pro
NM_001322051.2:c.484T>C NP_001308980.1:p.Ser162Pro
NR_136160.2:n.576T>C