Canonical Allele Identifier: CA9871630
Gene: ADA HGNC NCBI

Linked Data

dbSNP Id: rs377758134

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624262C>T , CM000682.2:g.44624262C>T GRCh38
NC_000020.10:g.43252903C>T , CM000682.1:g.43252903C>T GRCh37
NC_000020.9:g.42686317C>T NCBI36
NG_007385.1:g.32474G>A , LRG_16:g.32474G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.637G>A
ENST00000536076.2:c.393G>A ENSP00000512234.1:p.Leu131=
ENST00000536532.6:c.546G>A ENSP00000440946.1:p.Leu182=
ENST00000537820.2:c.546G>A ENSP00000441818.1:p.Leu182=
ENST00000539235.6:c.219-1184G>A ENSP00000446464.1:n.219-1184G>A
ENST00000695889.1:c.219-1332G>A ENSP00000512240.1:n.219-1332G>A
ENST00000695890.1:n.2349G>A
ENST00000695891.1:c.219-1332G>A ENSP00000512241.1:n.219-1332G>A
ENST00000695927.1:c.624G>A ENSP00000512270.1:p.Leu208=
ENST00000695949.1:c.543G>A ENSP00000512281.1:p.Leu181=
ENST00000695957.1:c.*37G>A ENSP00000512286.1:n.*37G>A
ENST00000695991.1:c.217-1332G>A ENSP00000512314.1:n.217-1332G>A
ENST00000695992.1:c.546G>A ENSP00000512315.1:p.Leu182=
ENST00000695993.1:c.546G>A ENSP00000512316.1:p.Leu182=
ENST00000695994.1:c.546G>A ENSP00000512317.1:p.Leu182=
ENST00000695995.1:c.217-1184G>A ENSP00000512318.1:n.217-1184G>A
ENST00000695996.1:n.617G>A
ENST00000695997.1:n.501G>A
ENST00000696003.1:n.638G>A
ENST00000696004.1:n.638G>A
ENST00000696005.1:c.68G>A
ENST00000696006.1:c.546G>A ENSP00000512325.1:p.Leu182=
ENST00000696007.1:c.397G>A ENSP00000512326.1:n.397G>A
ENST00000696008.1:n.1701G>A
ENST00000696009.1:n.1896G>A
ENST00000696017.1:c.543G>A ENSP00000512333.1:p.Leu181=
ENST00000696034.1:c.546G>A ENSP00000512343.1:p.Leu182=
ENST00000696035.1:n.656G>A
ENST00000696036.1:n.1236G>A
ENST00000696037.1:n.2223G>A
ENST00000696038.1:c.*292G>A ENSP00000512344.1:n.*292G>A
ENST00000696039.1:n.834G>A
ENST00000696058.1:c.546G>A ENSP00000512361.1:p.Leu182=
ENST00000696059.1:c.*491G>A ENSP00000512362.1:n.*491G>A
ENST00000696060.1:c.546G>A ENSP00000512363.1:p.Leu182=
ENST00000696061.1:c.543G>A ENSP00000512364.1:p.Leu181=
ENST00000696062.1:c.609G>A ENSP00000512365.1:p.Leu203=
ENST00000696063.1:c.621G>A ENSP00000512366.1:p.Leu207=
ENST00000696064.1:c.393G>A ENSP00000512367.1:p.Leu131=
ENST00000696065.1:c.66-1332G>A ENSP00000512368.1:n.66-1332G>A
ENST00000696074.1:n.162G>A
ENST00000696075.1:c.*516G>A ENSP00000512374.1:n.*516G>A
ENST00000696076.1:c.546G>A ENSP00000512375.1:p.Leu182=
ENST00000696077.1:c.543G>A ENSP00000512376.1:p.Leu181=
ENST00000696078.1:c.546G>A ENSP00000512377.1:p.Leu182=
ENST00000696079.1:c.546G>A ENSP00000512378.1:p.Leu182=
ENST00000696080.1:c.546G>A ENSP00000512379.1:p.Leu182=
ENST00000696081.1:n.665G>A
ENST00000696082.1:c.624G>A ENSP00000512380.1:p.Leu208=
ENST00000696083.1:n.1427G>A
ENST00000696084.1:n.647G>A
ENST00000696104.1:c.363-1332G>A ENSP00000512399.1:n.363-1332G>A
ENST00000696105.1:c.*87G>A ENSP00000512400.1:n.*87G>A
ENST00000372874.9:c.546G>A MANE Select ENSP00000361965.4:p.Leu182=
ENST00000372874.8:c.546G>A ENSP00000361965.4:p.Leu182=
ENST00000464097.5:n.220G>A
ENST00000492931.5:n.630G>A
ENST00000536532.5:c.546G>A ENSP00000440946.1:p.Leu182=
ENST00000537820.1:c.546G>A ENSP00000441818.1:p.Leu182=
ENST00000539235.5:c.219-1184G>A ENSP00000446464.1:n.219-1184G>A
NM_000022.2:c.546G>A , LRG_16t1:c.546G>A NP_000013.2:p.Leu182=
XM_005260236.2:c.546G>A XP_005260293.1:p.Leu182=
XM_011528478.1:c.141G>A XP_011526780.1:p.Leu47=
XM_011528479.1:c.141G>A XP_011526781.1:p.Leu47=
XR_244129.1:n.600G>A
NM_000022.3:c.546G>A NP_000013.2:p.Leu182=
NM_001322050.1:c.141G>A NP_001308979.1:p.Leu47=
NM_001322051.1:c.546G>A NP_001308980.1:p.Leu182=
NR_136160.1:n.697G>A
NM_000022.4:c.546G>A MANE Select NP_000013.2:p.Leu182=
NM_001322050.2:c.141G>A NP_001308979.1:p.Leu47=
NM_001322051.2:c.546G>A NP_001308980.1:p.Leu182=
NR_136160.2:n.638G>A