Canonical Allele Identifier: CA510593729
Gene: ADA HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.43252915T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624274T>A , CM000682.2:g.44624274T>A GRCh38
NC_000020.10:g.43252915T>A , CM000682.1:g.43252915T>A GRCh37
NC_000020.9:g.42686329T>A NCBI36
NG_007385.1:g.32462A>T , LRG_16:g.32462A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.625A>T
ENST00000536076.2:c.381A>T ENSP00000512234.1:p.Val127=
ENST00000536532.6:c.534A>T ENSP00000440946.1:p.Val178=
ENST00000537820.2:c.534A>T ENSP00000441818.1:p.Val178=
ENST00000539235.6:c.219-1196A>T ENSP00000446464.1:n.219-1196A>T
ENST00000695889.1:c.219-1344A>T ENSP00000512240.1:n.219-1344A>T
ENST00000695890.1:n.2337A>T
ENST00000695891.1:c.219-1344A>T ENSP00000512241.1:n.219-1344A>T
ENST00000695927.1:c.612A>T ENSP00000512270.1:p.Val204=
ENST00000695949.1:c.531A>T ENSP00000512281.1:p.Val177=
ENST00000695957.1:c.*25A>T ENSP00000512286.1:n.*25A>T
ENST00000695991.1:c.217-1344A>T ENSP00000512314.1:n.217-1344A>T
ENST00000695992.1:c.534A>T ENSP00000512315.1:p.Val178=
ENST00000695993.1:c.534A>T ENSP00000512316.1:p.Val178=
ENST00000695994.1:c.534A>T ENSP00000512317.1:p.Val178=
ENST00000695995.1:c.217-1196A>T ENSP00000512318.1:n.217-1196A>T
ENST00000695996.1:n.605A>T
ENST00000695997.1:n.489A>T
ENST00000696003.1:n.626A>T
ENST00000696004.1:n.626A>T
ENST00000696005.1:c.56A>T
ENST00000696006.1:c.534A>T ENSP00000512325.1:p.Val178=
ENST00000696007.1:c.385A>T ENSP00000512326.1:n.385A>T
ENST00000696008.1:n.1689A>T
ENST00000696009.1:n.1884A>T
ENST00000696017.1:c.531A>T ENSP00000512333.1:p.Val177=
ENST00000696034.1:c.534A>T ENSP00000512343.1:p.Val178=
ENST00000696035.1:n.644A>T
ENST00000696036.1:n.1224A>T
ENST00000696037.1:n.2211A>T
ENST00000696038.1:c.*280A>T ENSP00000512344.1:n.*280A>T
ENST00000696039.1:n.822A>T
ENST00000696058.1:c.534A>T ENSP00000512361.1:p.Val178=
ENST00000696059.1:c.*479A>T ENSP00000512362.1:n.*479A>T
ENST00000696060.1:c.534A>T ENSP00000512363.1:p.Val178=
ENST00000696061.1:c.531A>T ENSP00000512364.1:p.Val177=
ENST00000696062.1:c.597A>T ENSP00000512365.1:p.Val199=
ENST00000696063.1:c.609A>T ENSP00000512366.1:p.Val203=
ENST00000696064.1:c.381A>T ENSP00000512367.1:p.Val127=
ENST00000696065.1:c.66-1344A>T ENSP00000512368.1:n.66-1344A>T
ENST00000696074.1:n.150A>T
ENST00000696075.1:c.*504A>T ENSP00000512374.1:n.*504A>T
ENST00000696076.1:c.534A>T ENSP00000512375.1:p.Val178=
ENST00000696077.1:c.531A>T ENSP00000512376.1:p.Val177=
ENST00000696078.1:c.534A>T ENSP00000512377.1:p.Val178=
ENST00000696079.1:c.534A>T ENSP00000512378.1:p.Val178=
ENST00000696080.1:c.534A>T ENSP00000512379.1:p.Val178=
ENST00000696081.1:n.653A>T
ENST00000696082.1:c.612A>T ENSP00000512380.1:p.Val204=
ENST00000696083.1:n.1415A>T
ENST00000696084.1:n.635A>T
ENST00000696104.1:c.363-1344A>T ENSP00000512399.1:n.363-1344A>T
ENST00000696105.1:c.*75A>T ENSP00000512400.1:n.*75A>T
ENST00000372874.9:c.534A>T MANE Select ENSP00000361965.4:p.Val178=
ENST00000372874.8:c.534A>T ENSP00000361965.4:p.Val178=
ENST00000464097.5:n.208A>T
ENST00000492931.5:n.618A>T
ENST00000536532.5:c.534A>T ENSP00000440946.1:p.Val178=
ENST00000537820.1:c.534A>T ENSP00000441818.1:p.Val178=
ENST00000539235.5:c.219-1196A>T ENSP00000446464.1:n.219-1196A>T
NM_000022.2:c.534A>T , LRG_16t1:c.534A>T NP_000013.2:p.Val178=
XM_005260236.2:c.534A>T XP_005260293.1:p.Val178=
XM_011528478.1:c.129A>T XP_011526780.1:p.Val43=
XM_011528479.1:c.129A>T XP_011526781.1:p.Val43=
XR_244129.1:n.588A>T
NM_000022.3:c.534A>T NP_000013.2:p.Val178=
NM_001322050.1:c.129A>T NP_001308979.1:p.Val43=
NM_001322051.1:c.534A>T NP_001308980.1:p.Val178=
NR_136160.1:n.685A>T
NM_000022.4:c.534A>T MANE Select NP_000013.2:p.Val178=
NM_001322050.2:c.129A>T NP_001308979.1:p.Val43=
NM_001322051.2:c.534A>T NP_001308980.1:p.Val178=
NR_136160.2:n.626A>T