Canonical Allele Identifier: CA409120471

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623056T>C , CM000682.2:g.44623056T>C GRCh38
NC_000020.10:g.43251697T>C , CM000682.1:g.43251697T>C GRCh37
NC_000020.9:g.42685111T>C NCBI36
NG_007385.1:g.33680A>G , LRG_16:g.33680A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.720A>G (ADA)
ENST00000536076.2:c.476A>G (ADA) ENSP00000512234.1:p.His159Arg
ENST00000536532.6:c.629A>G (ADA) ENSP00000440946.1:p.His210Arg
ENST00000537820.2:c.607-126A>G (ADA) ENSP00000441818.1:n.607-126A>G
ENST00000539235.6:c.*13A>G (ADA) ENSP00000446464.1:n.*13A>G
ENST00000695889.1:c.219-126A>G (ADA) ENSP00000512240.1:n.219-126A>G
ENST00000695890.1:n.2432A>G (ADA)
ENST00000695891.1:c.219-126A>G (ADA) ENSP00000512241.1:n.219-126A>G
ENST00000695927.1:c.707A>G (ADA) ENSP00000512270.1:p.His236Arg
ENST00000695949.1:c.604-126A>G (ADA) ENSP00000512281.1:n.604-126A>G
ENST00000695957.1:c.*120A>G (ADA) ENSP00000512286.1:n.*120A>G
ENST00000695991.1:c.217-126A>G (ADA) ENSP00000512314.1:n.217-126A>G
ENST00000695992.1:c.629A>G (ADA) ENSP00000512315.1:p.His210Arg
ENST00000695993.1:c.629A>G (ADA) ENSP00000512316.1:p.His210Arg
ENST00000695994.1:c.629A>G (ADA) ENSP00000512317.1:p.His210Arg
ENST00000695995.1:c.239A>G (ADA) ENSP00000512318.1:p.His80Arg
ENST00000695996.1:n.700A>G (ADA)
ENST00000696003.1:n.721A>G (ADA)
ENST00000696004.1:n.721A>G (ADA)
ENST00000696005.1:c.129-126A>G (ADA)
ENST00000696006.1:c.607-126A>G (ADA) ENSP00000512325.1:n.607-126A>G
ENST00000696007.1:c.480A>G (ADA) ENSP00000512326.1:n.480A>G
ENST00000696008.1:n.2907A>G (ADA)
ENST00000696017.1:c.626A>G (ADA) ENSP00000512333.1:p.His209Arg
ENST00000696034.1:c.629A>G (ADA) ENSP00000512343.1:p.His210Arg
ENST00000696035.1:n.739A>G (ADA)
ENST00000696036.1:n.1319A>G (ADA)
ENST00000696037.1:n.2306A>G (ADA)
ENST00000696038.1:c.*375A>G (ADA) ENSP00000512344.1:n.*375A>G
ENST00000696039.1:n.917A>G (ADA)
ENST00000696058.1:c.626A>G (ADA) ENSP00000512361.1:p.His209Arg
ENST00000696059.1:c.*574A>G (ADA) ENSP00000512362.1:n.*574A>G
ENST00000696060.1:c.698A>G (ADA) ENSP00000512363.1:p.His233Arg
ENST00000696061.1:c.626A>G (ADA) ENSP00000512364.1:p.His209Arg
ENST00000696062.1:c.692A>G (ADA) ENSP00000512365.1:p.His231Arg
ENST00000696063.1:c.704A>G (ADA) ENSP00000512366.1:p.His235Arg
ENST00000696064.1:c.476A>G (ADA) ENSP00000512367.1:p.His159Arg
ENST00000696065.1:c.66-126A>G (ADA) ENSP00000512368.1:n.66-126A>G
ENST00000696073.1:n.864A>G (ADA)
ENST00000696074.1:n.245A>G (ADA)
ENST00000696075.1:c.*599A>G (ADA) ENSP00000512374.1:n.*599A>G
ENST00000696076.1:c.698A>G (ADA) ENSP00000512375.1:p.His233Arg
ENST00000696077.1:c.623A>G (ADA) ENSP00000512376.1:p.His208Arg
ENST00000696078.1:c.626A>G (ADA) ENSP00000512377.1:p.His209Arg
ENST00000696079.1:c.626A>G (ADA) ENSP00000512378.1:p.His209Arg
ENST00000696080.1:c.629A>G (ADA) ENSP00000512379.1:p.His210Arg
ENST00000696081.1:n.748A>G (ADA)
ENST00000696082.1:c.704A>G (ADA) ENSP00000512380.1:p.His235Arg
ENST00000696083.1:n.1510A>G (ADA)
ENST00000696084.1:n.730A>G (ADA)
ENST00000696104.1:c.363-126A>G (ADA) ENSP00000512399.1:n.363-126A>G
ENST00000696105.1:c.*170A>G (ADA) ENSP00000512400.1:n.*170A>G
ENST00000372874.9:c.629A>G (ADA) MANE Select ENSP00000361965.4:p.His210Arg
ENST00000372874.8:c.629A>G (ADA) ENSP00000361965.4:p.His210Arg
ENST00000372887.5:c.152-877T>C (PKIG) ENSP00000361978.1:n.152-877T>C
ENST00000464097.5:n.303A>G (ADA)
ENST00000492931.5:n.713A>G (ADA)
ENST00000536532.5:c.629A>G (ADA) ENSP00000440946.1:p.His210Arg
ENST00000537820.1:c.607-126A>G (ADA) ENSP00000441818.1:n.607-126A>G
ENST00000539235.5:c.*13A>G (ADA) ENSP00000446464.1:n.*13A>G
NM_000022.2:c.629A>G , LRG_16t1:c.629A>G (ADA) NP_000013.2:p.His210Arg
XM_005260236.2:c.607-126A>G (ADA) XP_005260293.1:n.607-126A>G
XM_011528478.1:c.224A>G (ADA) XP_011526780.1:p.His75Arg
XM_011528479.1:c.224A>G (ADA) XP_011526781.1:p.His75Arg
XR_244129.1:n.683A>G (ADA)
NM_000022.3:c.629A>G (ADA) NP_000013.2:p.His210Arg
NM_001322050.1:c.224A>G (ADA) NP_001308979.1:p.His75Arg
NM_001322051.1:c.607-126A>G (ADA) NP_001308980.1:n.607-126A>G
NR_136160.1:n.780A>G (ADA)
NM_000022.4:c.629A>G (ADA) MANE Select NP_000013.2:p.His210Arg
NM_001322050.2:c.224A>G (ADA) NP_001308979.1:p.His75Arg
NM_001322051.2:c.607-126A>G (ADA) NP_001308980.1:n.607-126A>G
NR_136160.2:n.721A>G (ADA)