Canonical Allele Identifier: CA2365862057
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44636380C= , CM000682.2:g.44636380C= GRCh38
NC_000020.10:g.43265021C= , CM000682.1:g.43265021C= GRCh37
NC_000020.9:g.42698435C= NCBI36
NG_007385.1:g.20356G= , LRG_16:g.20356G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.125-92G=
ENST00000536076.2:c.-120-92G= ENSP00000512234.1:n.-120-92G=
ENST00000536532.6:c.34-92G= ENSP00000440946.1:n.34-92G=
ENST00000537820.2:c.34-92G= ENSP00000441818.1:n.34-92G=
ENST00000539235.6:c.34-92G= ENSP00000446464.1:n.34-92G=
ENST00000695889.1:c.34-92G= ENSP00000512240.1:n.34-92G=
ENST00000695891.1:c.34-92G= ENSP00000512241.1:n.34-92G=
ENST00000695927.1:c.112-92G= ENSP00000512270.1:n.112-92G=
ENST00000695949.1:c.34-92G= ENSP00000512281.1:n.34-92G=
ENST00000695957.1:c.34-92G= ENSP00000512286.1:n.34-92G=
ENST00000695991.1:c.34-92G= ENSP00000512314.1:n.34-92G=
ENST00000695992.1:c.34-92G= ENSP00000512315.1:n.34-92G=
ENST00000695993.1:c.34-92G= ENSP00000512316.1:n.34-92G=
ENST00000695994.1:c.34-92G= ENSP00000512317.1:n.34-92G=
ENST00000695995.1:c.34-92G= ENSP00000512318.1:n.34-92G=
ENST00000695996.1:n.105-92G=
ENST00000695997.1:n.105-92G=
ENST00000696003.1:n.126-92G=
ENST00000696004.1:n.126-92G=
ENST00000696006.1:c.34-92G= ENSP00000512325.1:n.34-92G=
ENST00000696009.1:n.145-92G=
ENST00000696010.1:n.147-92G=
ENST00000696017.1:c.34-92G= ENSP00000512333.1:n.34-92G=
ENST00000696034.1:c.34-92G= ENSP00000512343.1:n.34-92G=
ENST00000696038.1:c.34-92G= ENSP00000512344.1:n.34-92G=
ENST00000696039.1:n.322-92G=
ENST00000696058.1:c.34-92G= ENSP00000512361.1:n.34-92G=
ENST00000696059.1:c.141-92G= ENSP00000512362.1:n.141-92G=
ENST00000696060.1:c.34-92G= ENSP00000512363.1:n.34-92G=
ENST00000696061.1:c.34-92G= ENSP00000512364.1:n.34-92G=
ENST00000696062.1:c.97-92G= ENSP00000512365.1:n.97-92G=
ENST00000696063.1:c.109-92G= ENSP00000512366.1:n.109-92G=
ENST00000696064.1:c.-117-92G= ENSP00000512367.1:n.-117-92G=
ENST00000696065.1:c.-120-92G= ENSP00000512368.1:n.-120-92G=
ENST00000696075.1:c.34-92G= ENSP00000512374.1:n.34-92G=
ENST00000696076.1:c.34-92G= ENSP00000512375.1:n.34-92G=
ENST00000696077.1:c.34-92G= ENSP00000512376.1:n.34-92G=
ENST00000696078.1:c.34-92G= ENSP00000512377.1:n.34-92G=
ENST00000696079.1:c.34-92G= ENSP00000512378.1:n.34-92G=
ENST00000696080.1:c.34-92G= ENSP00000512379.1:n.34-92G=
ENST00000696082.1:c.112-92G= ENSP00000512380.1:n.112-92G=
ENST00000696084.1:n.135-92G=
ENST00000696104.1:c.34-92G= ENSP00000512399.1:n.34-92G=
ENST00000696105.1:c.34-92G= ENSP00000512400.1:n.34-92G=
ENST00000372874.9:c.34-92G= MANE Select ENSP00000361965.4:n.34-92G=
ENST00000372874.8:c.34-92G= ENSP00000361965.4:n.34-92G=
ENST00000492931.5:n.118-92G=
ENST00000535573.1:n.333-92G=
ENST00000536076.1:n.214-92G=
ENST00000536532.5:c.34-92G= ENSP00000440946.1:n.34-92G=
ENST00000537820.1:c.34-92G= ENSP00000441818.1:n.34-92G=
ENST00000539235.5:c.34-92G= ENSP00000446464.1:n.34-92G=
ENST00000545776.5:n.88-92G=
NM_000022.2:c.34-92G= , LRG_16t1:c.34-92G= NP_000013.2:n.34-92G=
XM_005260236.2:c.34-92G= XP_005260293.1:n.34-92G=
XM_011528478.1:c.-256-92G= XP_011526780.1:n.-256-92G=
XM_011528479.1:c.-256-92G= XP_011526781.1:n.-256-92G=
XR_244129.1:n.88-92G=
NM_000022.3:c.34-92G= NP_000013.2:n.34-92G=
NM_001322050.1:c.-256-92G= NP_001308979.1:n.-256-92G=
NM_001322051.1:c.34-92G= NP_001308980.1:n.34-92G=
NR_136160.1:n.185-92G=
NM_000022.4:c.34-92G= MANE Select NP_000013.2:n.34-92G=
NM_001322050.2:c.-256-92G= NP_001308979.1:n.-256-92G=
NM_001322051.2:c.34-92G= NP_001308980.1:n.34-92G=
NR_136160.2:n.126-92G=