Canonical Allele Identifier: CA2365861986
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44636234A= , CM000682.2:g.44636234A= GRCh38
NC_000020.10:g.43264875A= , CM000682.1:g.43264875A= GRCh37
NC_000020.9:g.42698289A= NCBI36
NG_007385.1:g.20502T= , LRG_16:g.20502T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.179T=
ENST00000536076.2:c.-66T= ENSP00000512234.1:n.-66T=
ENST00000536532.6:c.88T= ENSP00000440946.1:p.Tyr30=
ENST00000537820.2:c.88T= ENSP00000441818.1:p.Tyr30=
ENST00000539235.6:c.88T= ENSP00000446464.1:p.Tyr30=
ENST00000695889.1:c.88T= ENSP00000512240.1:p.Tyr30=
ENST00000695891.1:c.88T= ENSP00000512241.1:p.Tyr30=
ENST00000695927.1:c.166T= ENSP00000512270.1:p.Tyr56=
ENST00000695949.1:c.88T= ENSP00000512281.1:p.Tyr30=
ENST00000695957.1:c.88T= ENSP00000512286.1:p.Tyr30=
ENST00000695991.1:c.88T= ENSP00000512314.1:p.Tyr30=
ENST00000695992.1:c.88T= ENSP00000512315.1:p.Tyr30=
ENST00000695993.1:c.88T= ENSP00000512316.1:p.Tyr30=
ENST00000695994.1:c.88T= ENSP00000512317.1:p.Tyr30=
ENST00000695995.1:c.88T= ENSP00000512318.1:p.Tyr30=
ENST00000695996.1:n.159T=
ENST00000695997.1:n.159T=
ENST00000696003.1:n.180T=
ENST00000696004.1:n.180T=
ENST00000696006.1:c.88T= ENSP00000512325.1:p.Tyr30=
ENST00000696007.1:c.55T= ENSP00000512326.1:p.Tyr19=
ENST00000696009.1:n.199T=
ENST00000696010.1:n.201T=
ENST00000696017.1:c.88T= ENSP00000512333.1:p.Tyr30=
ENST00000696034.1:c.88T= ENSP00000512343.1:p.Tyr30=
ENST00000696038.1:c.88T= ENSP00000512344.1:p.Tyr30=
ENST00000696039.1:n.376T=
ENST00000696058.1:c.88T= ENSP00000512361.1:p.Tyr30=
ENST00000696059.1:c.*33T= ENSP00000512362.1:n.*33T=
ENST00000696060.1:c.88T= ENSP00000512363.1:p.Tyr30=
ENST00000696061.1:c.88T= ENSP00000512364.1:p.Tyr30=
ENST00000696062.1:c.151T= ENSP00000512365.1:p.Tyr51=
ENST00000696063.1:c.163T= ENSP00000512366.1:p.Tyr55=
ENST00000696064.1:c.-63T= ENSP00000512367.1:n.-63T=
ENST00000696065.1:c.-66T= ENSP00000512368.1:n.-66T=
ENST00000696075.1:c.88T= ENSP00000512374.1:p.Tyr30=
ENST00000696076.1:c.88T= ENSP00000512375.1:p.Tyr30=
ENST00000696077.1:c.88T= ENSP00000512376.1:p.Tyr30=
ENST00000696078.1:c.88T= ENSP00000512377.1:p.Tyr30=
ENST00000696079.1:c.88T= ENSP00000512378.1:p.Tyr30=
ENST00000696080.1:c.88T= ENSP00000512379.1:p.Tyr30=
ENST00000696082.1:c.166T= ENSP00000512380.1:p.Tyr56=
ENST00000696084.1:n.189T=
ENST00000696104.1:c.88T= ENSP00000512399.1:p.Tyr30=
ENST00000696105.1:c.88T= ENSP00000512400.1:p.Tyr30=
ENST00000372874.9:c.88T= MANE Select ENSP00000361965.4:p.Tyr30=
ENST00000372874.8:c.88T= ENSP00000361965.4:p.Tyr30=
ENST00000492931.5:n.172T=
ENST00000535573.1:n.387T=
ENST00000536076.1:n.268T=
ENST00000536532.5:c.88T= ENSP00000440946.1:p.Tyr30=
ENST00000537820.1:c.88T= ENSP00000441818.1:p.Tyr30=
ENST00000539235.5:c.88T= ENSP00000446464.1:p.Tyr30=
ENST00000545776.5:n.142T=
NM_000022.2:c.88T= , LRG_16t1:c.88T= NP_000013.2:p.Tyr30=
XM_005260236.2:c.88T= XP_005260293.1:p.Tyr30=
XM_011528478.1:c.-202T= XP_011526780.1:n.-202T=
XM_011528479.1:c.-202T= XP_011526781.1:n.-202T=
XR_244129.1:n.142T=
NM_000022.3:c.88T= NP_000013.2:p.Tyr30=
NM_001322050.1:c.-202T= NP_001308979.1:n.-202T=
NM_001322051.1:c.88T= NP_001308980.1:p.Tyr30=
NR_136160.1:n.239T=
NM_000022.4:c.88T= MANE Select NP_000013.2:p.Tyr30=
NM_001322050.2:c.-202T= NP_001308979.1:n.-202T=
NM_001322051.2:c.88T= NP_001308980.1:p.Tyr30=
NR_136160.2:n.180T=