Canonical Allele Identifier: CA2365856557
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624260G= , CM000682.2:g.44624260G= GRCh38
NC_000020.10:g.43252901G= , CM000682.1:g.43252901G= GRCh37
NC_000020.9:g.42686315G= NCBI36
NG_007385.1:g.32476C= , LRG_16:g.32476C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.639C=
ENST00000536076.2:c.395C= ENSP00000512234.1:p.Ala132=
ENST00000536532.6:c.548C= ENSP00000440946.1:p.Ala183=
ENST00000537820.2:c.548C= ENSP00000441818.1:p.Ala183=
ENST00000539235.6:c.219-1182C= ENSP00000446464.1:n.219-1182C=
ENST00000695889.1:c.219-1330C= ENSP00000512240.1:n.219-1330C=
ENST00000695890.1:n.2351C=
ENST00000695891.1:c.219-1330C= ENSP00000512241.1:n.219-1330C=
ENST00000695927.1:c.626C= ENSP00000512270.1:p.Ala209=
ENST00000695949.1:c.545C= ENSP00000512281.1:p.Ala182=
ENST00000695957.1:c.*39C= ENSP00000512286.1:n.*39C=
ENST00000695991.1:c.217-1330C= ENSP00000512314.1:n.217-1330C=
ENST00000695992.1:c.548C= ENSP00000512315.1:p.Ala183=
ENST00000695993.1:c.548C= ENSP00000512316.1:p.Ala183=
ENST00000695994.1:c.548C= ENSP00000512317.1:p.Ala183=
ENST00000695995.1:c.217-1182C= ENSP00000512318.1:n.217-1182C=
ENST00000695996.1:n.619C=
ENST00000695997.1:n.503C=
ENST00000696003.1:n.640C=
ENST00000696004.1:n.640C=
ENST00000696005.1:c.70C=
ENST00000696006.1:c.548C= ENSP00000512325.1:p.Ala183=
ENST00000696007.1:c.399C= ENSP00000512326.1:n.399C=
ENST00000696008.1:n.1703C=
ENST00000696009.1:n.1898C=
ENST00000696017.1:c.545C= ENSP00000512333.1:p.Ala182=
ENST00000696034.1:c.548C= ENSP00000512343.1:p.Ala183=
ENST00000696035.1:n.658C=
ENST00000696036.1:n.1238C=
ENST00000696037.1:n.2225C=
ENST00000696038.1:c.*294C= ENSP00000512344.1:n.*294C=
ENST00000696039.1:n.836C=
ENST00000696058.1:c.548C= ENSP00000512361.1:p.Ala183=
ENST00000696059.1:c.*493C= ENSP00000512362.1:n.*493C=
ENST00000696060.1:c.548C= ENSP00000512363.1:p.Ala183=
ENST00000696061.1:c.545C= ENSP00000512364.1:p.Ala182=
ENST00000696062.1:c.611C= ENSP00000512365.1:p.Ala204=
ENST00000696063.1:c.623C= ENSP00000512366.1:p.Ala208=
ENST00000696064.1:c.395C= ENSP00000512367.1:p.Ala132=
ENST00000696065.1:c.66-1330C= ENSP00000512368.1:n.66-1330C=
ENST00000696074.1:n.164C=
ENST00000696075.1:c.*518C= ENSP00000512374.1:n.*518C=
ENST00000696076.1:c.548C= ENSP00000512375.1:p.Ala183=
ENST00000696077.1:c.545C= ENSP00000512376.1:p.Ala182=
ENST00000696078.1:c.548C= ENSP00000512377.1:p.Ala183=
ENST00000696079.1:c.548C= ENSP00000512378.1:p.Ala183=
ENST00000696080.1:c.548C= ENSP00000512379.1:p.Ala183=
ENST00000696081.1:n.667C=
ENST00000696082.1:c.626C= ENSP00000512380.1:p.Ala209=
ENST00000696083.1:n.1429C=
ENST00000696084.1:n.649C=
ENST00000696104.1:c.363-1330C= ENSP00000512399.1:n.363-1330C=
ENST00000696105.1:c.*89C= ENSP00000512400.1:n.*89C=
ENST00000372874.9:c.548C= MANE Select ENSP00000361965.4:p.Ala183=
ENST00000372874.8:c.548C= ENSP00000361965.4:p.Ala183=
ENST00000464097.5:n.222C=
ENST00000492931.5:n.632C=
ENST00000536532.5:c.548C= ENSP00000440946.1:p.Ala183=
ENST00000537820.1:c.548C= ENSP00000441818.1:p.Ala183=
ENST00000539235.5:c.219-1182C= ENSP00000446464.1:n.219-1182C=
NM_000022.2:c.548C= , LRG_16t1:c.548C= NP_000013.2:p.Ala183=
XM_005260236.2:c.548C= XP_005260293.1:p.Ala183=
XM_011528478.1:c.143C= XP_011526780.1:p.Ala48=
XM_011528479.1:c.143C= XP_011526781.1:p.Ala48=
XR_244129.1:n.602C=
NM_000022.3:c.548C= NP_000013.2:p.Ala183=
NM_001322050.1:c.143C= NP_001308979.1:p.Ala48=
NM_001322051.1:c.548C= NP_001308980.1:p.Ala183=
NR_136160.1:n.699C=
NM_000022.4:c.548C= MANE Select NP_000013.2:p.Ala183=
NM_001322050.2:c.143C= NP_001308979.1:p.Ala48=
NM_001322051.2:c.548C= NP_001308980.1:p.Ala183=
NR_136160.2:n.640C=