Canonical Allele Identifier: CA2652991988
Gene: ADA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44636299dup , CM000682.2:g.44636299dup GRCh38
NC_000020.10:g.43264940dup , CM000682.1:g.43264940dup GRCh37
NC_000020.9:g.42698354dup NCBI36
NG_007385.1:g.20441dup , LRG_16:g.20441dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.125-7dup
ENST00000536076.2:c.-120-7dup ENSP00000512234.1:n.-120-7dup
ENST00000536532.6:c.34-7dup ENSP00000440946.1:n.34-7dup
ENST00000537820.2:c.34-7dup ENSP00000441818.1:n.34-7dup
ENST00000539235.6:c.34-7dup ENSP00000446464.1:n.34-7dup
ENST00000695889.1:c.34-7dup ENSP00000512240.1:n.34-7dup
ENST00000695891.1:c.34-7dup ENSP00000512241.1:n.34-7dup
ENST00000695927.1:c.112-7dup ENSP00000512270.1:n.112-7dup
ENST00000695949.1:c.34-7dup ENSP00000512281.1:n.34-7dup
ENST00000695957.1:c.34-7dup ENSP00000512286.1:n.34-7dup
ENST00000695991.1:c.34-7dup ENSP00000512314.1:n.34-7dup
ENST00000695992.1:c.34-7dup ENSP00000512315.1:n.34-7dup
ENST00000695993.1:c.34-7dup ENSP00000512316.1:n.34-7dup
ENST00000695994.1:c.34-7dup ENSP00000512317.1:n.34-7dup
ENST00000695995.1:c.34-7dup ENSP00000512318.1:n.34-7dup
ENST00000695996.1:n.105-7dup
ENST00000695997.1:n.105-7dup
ENST00000696003.1:n.126-7dup
ENST00000696004.1:n.126-7dup
ENST00000696006.1:c.34-7dup ENSP00000512325.1:n.34-7dup
ENST00000696009.1:n.145-7dup
ENST00000696010.1:n.147-7dup
ENST00000696017.1:c.34-7dup ENSP00000512333.1:n.34-7dup
ENST00000696034.1:c.34-7dup ENSP00000512343.1:n.34-7dup
ENST00000696038.1:c.34-7dup ENSP00000512344.1:n.34-7dup
ENST00000696039.1:n.322-7dup
ENST00000696058.1:c.34-7dup ENSP00000512361.1:n.34-7dup
ENST00000696059.1:c.141-7dup ENSP00000512362.1:n.141-7dup
ENST00000696060.1:c.34-7dup ENSP00000512363.1:n.34-7dup
ENST00000696061.1:c.34-7dup ENSP00000512364.1:n.34-7dup
ENST00000696062.1:c.97-7dup ENSP00000512365.1:n.97-7dup
ENST00000696063.1:c.109-7dup ENSP00000512366.1:n.109-7dup
ENST00000696064.1:c.-117-7dup ENSP00000512367.1:n.-117-7dup
ENST00000696065.1:c.-120-7dup ENSP00000512368.1:n.-120-7dup
ENST00000696075.1:c.34-7dup ENSP00000512374.1:n.34-7dup
ENST00000696076.1:c.34-7dup ENSP00000512375.1:n.34-7dup
ENST00000696077.1:c.34-7dup ENSP00000512376.1:n.34-7dup
ENST00000696078.1:c.34-7dup ENSP00000512377.1:n.34-7dup
ENST00000696079.1:c.34-7dup ENSP00000512378.1:n.34-7dup
ENST00000696080.1:c.34-7dup ENSP00000512379.1:n.34-7dup
ENST00000696082.1:c.112-7dup ENSP00000512380.1:n.112-7dup
ENST00000696084.1:n.135-7dup
ENST00000696104.1:c.34-7dup ENSP00000512399.1:n.34-7dup
ENST00000696105.1:c.34-7dup ENSP00000512400.1:n.34-7dup
ENST00000372874.9:c.34-7dup MANE Select ENSP00000361965.4:n.34-7dup
ENST00000372874.8:c.34-7dup ENSP00000361965.4:n.34-7dup
ENST00000492931.5:n.118-7dup
ENST00000535573.1:n.333-7dup
ENST00000536076.1:n.214-7dup
ENST00000536532.5:c.34-7dup ENSP00000440946.1:n.34-7dup
ENST00000537820.1:c.34-7dup ENSP00000441818.1:n.34-7dup
ENST00000539235.5:c.34-7dup ENSP00000446464.1:n.34-7dup
ENST00000545776.5:n.88-7dup
NM_000022.2:c.34-7dup , LRG_16t1:c.34-7dup NP_000013.2:n.34-7dup
XM_005260236.2:c.34-7dup XP_005260293.1:n.34-7dup
XM_011528478.1:c.-256-7dup XP_011526780.1:n.-256-7dup
XM_011528479.1:c.-256-7dup XP_011526781.1:n.-256-7dup
XR_244129.1:n.88-7dup
NM_000022.3:c.34-7dup NP_000013.2:n.34-7dup
NM_001322050.1:c.-256-7dup NP_001308979.1:n.-256-7dup
NM_001322051.1:c.34-7dup NP_001308980.1:n.34-7dup
NR_136160.1:n.185-7dup
NM_000022.4:c.34-7dup MANE Select NP_000013.2:n.34-7dup
NM_001322050.2:c.-256-7dup NP_001308979.1:n.-256-7dup
NM_001322051.2:c.34-7dup NP_001308980.1:n.34-7dup
NR_136160.2:n.126-7dup