Canonical Allele Identifier: CA409120468

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623055G>C , CM000682.2:g.44623055G>C GRCh38
NC_000020.10:g.43251696G>C , CM000682.1:g.43251696G>C GRCh37
NC_000020.9:g.42685110G>C NCBI36
NG_007385.1:g.33681C>G , LRG_16:g.33681C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.721C>G (ADA)
ENST00000536076.2:c.477C>G (ADA) ENSP00000512234.1:p.His159Gln
ENST00000536532.6:c.630C>G (ADA) ENSP00000440946.1:p.His210Gln
ENST00000537820.2:c.607-125C>G (ADA) ENSP00000441818.1:n.607-125C>G
ENST00000539235.6:c.*14C>G (ADA) ENSP00000446464.1:n.*14C>G
ENST00000695889.1:c.219-125C>G (ADA) ENSP00000512240.1:n.219-125C>G
ENST00000695890.1:n.2433C>G (ADA)
ENST00000695891.1:c.219-125C>G (ADA) ENSP00000512241.1:n.219-125C>G
ENST00000695927.1:c.708C>G (ADA) ENSP00000512270.1:p.His236Gln
ENST00000695949.1:c.604-125C>G (ADA) ENSP00000512281.1:n.604-125C>G
ENST00000695957.1:c.*121C>G (ADA) ENSP00000512286.1:n.*121C>G
ENST00000695991.1:c.217-125C>G (ADA) ENSP00000512314.1:n.217-125C>G
ENST00000695992.1:c.630C>G (ADA) ENSP00000512315.1:p.His210Gln
ENST00000695993.1:c.630C>G (ADA) ENSP00000512316.1:p.His210Gln
ENST00000695994.1:c.630C>G (ADA) ENSP00000512317.1:p.His210Gln
ENST00000695995.1:c.240C>G (ADA) ENSP00000512318.1:p.His80Gln
ENST00000695996.1:n.701C>G (ADA)
ENST00000696003.1:n.722C>G (ADA)
ENST00000696004.1:n.722C>G (ADA)
ENST00000696005.1:c.129-125C>G (ADA)
ENST00000696006.1:c.607-125C>G (ADA) ENSP00000512325.1:n.607-125C>G
ENST00000696007.1:c.481C>G (ADA) ENSP00000512326.1:n.481C>G
ENST00000696008.1:n.2908C>G (ADA)
ENST00000696017.1:c.627C>G (ADA) ENSP00000512333.1:p.His209Gln
ENST00000696034.1:c.630C>G (ADA) ENSP00000512343.1:p.His210Gln
ENST00000696035.1:n.740C>G (ADA)
ENST00000696036.1:n.1320C>G (ADA)
ENST00000696037.1:n.2307C>G (ADA)
ENST00000696038.1:c.*376C>G (ADA) ENSP00000512344.1:n.*376C>G
ENST00000696039.1:n.918C>G (ADA)
ENST00000696058.1:c.627C>G (ADA) ENSP00000512361.1:p.His209Gln
ENST00000696059.1:c.*575C>G (ADA) ENSP00000512362.1:n.*575C>G
ENST00000696060.1:c.699C>G (ADA) ENSP00000512363.1:p.His233Gln
ENST00000696061.1:c.627C>G (ADA) ENSP00000512364.1:p.His209Gln
ENST00000696062.1:c.693C>G (ADA) ENSP00000512365.1:p.His231Gln
ENST00000696063.1:c.705C>G (ADA) ENSP00000512366.1:p.His235Gln
ENST00000696064.1:c.477C>G (ADA) ENSP00000512367.1:p.His159Gln
ENST00000696065.1:c.66-125C>G (ADA) ENSP00000512368.1:n.66-125C>G
ENST00000696073.1:n.865C>G (ADA)
ENST00000696074.1:n.246C>G (ADA)
ENST00000696075.1:c.*600C>G (ADA) ENSP00000512374.1:n.*600C>G
ENST00000696076.1:c.699C>G (ADA) ENSP00000512375.1:p.His233Gln
ENST00000696077.1:c.624C>G (ADA) ENSP00000512376.1:p.His208Gln
ENST00000696078.1:c.627C>G (ADA) ENSP00000512377.1:p.His209Gln
ENST00000696079.1:c.627C>G (ADA) ENSP00000512378.1:p.His209Gln
ENST00000696080.1:c.630C>G (ADA) ENSP00000512379.1:p.His210Gln
ENST00000696081.1:n.749C>G (ADA)
ENST00000696082.1:c.705C>G (ADA) ENSP00000512380.1:p.His235Gln
ENST00000696083.1:n.1511C>G (ADA)
ENST00000696084.1:n.731C>G (ADA)
ENST00000696104.1:c.363-125C>G (ADA) ENSP00000512399.1:n.363-125C>G
ENST00000696105.1:c.*171C>G (ADA) ENSP00000512400.1:n.*171C>G
ENST00000372874.9:c.630C>G (ADA) MANE Select ENSP00000361965.4:p.His210Gln
ENST00000372874.8:c.630C>G (ADA) ENSP00000361965.4:p.His210Gln
ENST00000372887.5:c.152-878G>C (PKIG) ENSP00000361978.1:n.152-878G>C
ENST00000464097.5:n.304C>G (ADA)
ENST00000492931.5:n.714C>G (ADA)
ENST00000536532.5:c.630C>G (ADA) ENSP00000440946.1:p.His210Gln
ENST00000537820.1:c.607-125C>G (ADA) ENSP00000441818.1:n.607-125C>G
ENST00000539235.5:c.*14C>G (ADA) ENSP00000446464.1:n.*14C>G
NM_000022.2:c.630C>G , LRG_16t1:c.630C>G (ADA) NP_000013.2:p.His210Gln
XM_005260236.2:c.607-125C>G (ADA) XP_005260293.1:n.607-125C>G
XM_011528478.1:c.225C>G (ADA) XP_011526780.1:p.His75Gln
XM_011528479.1:c.225C>G (ADA) XP_011526781.1:p.His75Gln
XR_244129.1:n.684C>G (ADA)
NM_000022.3:c.630C>G (ADA) NP_000013.2:p.His210Gln
NM_001322050.1:c.225C>G (ADA) NP_001308979.1:p.His75Gln
NM_001322051.1:c.607-125C>G (ADA) NP_001308980.1:n.607-125C>G
NR_136160.1:n.781C>G (ADA)
NM_000022.4:c.630C>G (ADA) MANE Select NP_000013.2:p.His210Gln
NM_001322050.2:c.225C>G (ADA) NP_001308979.1:p.His75Gln
NM_001322051.2:c.607-125C>G (ADA) NP_001308980.1:n.607-125C>G
NR_136160.2:n.722C>G (ADA)