Canonical Allele Identifier: CA409120493

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623066T>C , CM000682.2:g.44623066T>C GRCh38
NC_000020.10:g.43251707T>C , CM000682.1:g.43251707T>C GRCh37
NC_000020.9:g.42685121T>C NCBI36
NG_007385.1:g.33670A>G , LRG_16:g.33670A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.710A>G (ADA)
ENST00000536076.2:c.466A>G (ADA) ENSP00000512234.1:p.Ser156Gly
ENST00000536532.6:c.619A>G (ADA) ENSP00000440946.1:p.Ser207Gly
ENST00000537820.2:c.607-136A>G (ADA) ENSP00000441818.1:n.607-136A>G
ENST00000539235.6:c.*3A>G (ADA) ENSP00000446464.1:n.*3A>G
ENST00000695889.1:c.219-136A>G (ADA) ENSP00000512240.1:n.219-136A>G
ENST00000695890.1:n.2422A>G (ADA)
ENST00000695891.1:c.219-136A>G (ADA) ENSP00000512241.1:n.219-136A>G
ENST00000695927.1:c.697A>G (ADA) ENSP00000512270.1:p.Ser233Gly
ENST00000695949.1:c.604-136A>G (ADA) ENSP00000512281.1:n.604-136A>G
ENST00000695957.1:c.*110A>G (ADA) ENSP00000512286.1:n.*110A>G
ENST00000695991.1:c.217-136A>G (ADA) ENSP00000512314.1:n.217-136A>G
ENST00000695992.1:c.619A>G (ADA) ENSP00000512315.1:p.Ser207Gly
ENST00000695993.1:c.619A>G (ADA) ENSP00000512316.1:p.Ser207Gly
ENST00000695994.1:c.619A>G (ADA) ENSP00000512317.1:p.Ser207Gly
ENST00000695995.1:c.229A>G (ADA) ENSP00000512318.1:p.Ser77Gly
ENST00000695996.1:n.690A>G (ADA)
ENST00000696003.1:n.711A>G (ADA)
ENST00000696004.1:n.711A>G (ADA)
ENST00000696005.1:c.129-136A>G (ADA)
ENST00000696006.1:c.607-136A>G (ADA) ENSP00000512325.1:n.607-136A>G
ENST00000696007.1:c.470A>G (ADA) ENSP00000512326.1:n.470A>G
ENST00000696008.1:n.2897A>G (ADA)
ENST00000696017.1:c.616A>G (ADA) ENSP00000512333.1:p.Ser206Gly
ENST00000696034.1:c.619A>G (ADA) ENSP00000512343.1:p.Ser207Gly
ENST00000696035.1:n.729A>G (ADA)
ENST00000696036.1:n.1309A>G (ADA)
ENST00000696037.1:n.2296A>G (ADA)
ENST00000696038.1:c.*365A>G (ADA) ENSP00000512344.1:n.*365A>G
ENST00000696039.1:n.907A>G (ADA)
ENST00000696058.1:c.616A>G (ADA) ENSP00000512361.1:p.Ser206Gly
ENST00000696059.1:c.*564A>G (ADA) ENSP00000512362.1:n.*564A>G
ENST00000696060.1:c.688A>G (ADA) ENSP00000512363.1:p.Ser230Gly
ENST00000696061.1:c.616A>G (ADA) ENSP00000512364.1:p.Ser206Gly
ENST00000696062.1:c.682A>G (ADA) ENSP00000512365.1:p.Ser228Gly
ENST00000696063.1:c.694A>G (ADA) ENSP00000512366.1:p.Ser232Gly
ENST00000696064.1:c.466A>G (ADA) ENSP00000512367.1:p.Ser156Gly
ENST00000696065.1:c.66-136A>G (ADA) ENSP00000512368.1:n.66-136A>G
ENST00000696073.1:n.854A>G (ADA)
ENST00000696074.1:n.235A>G (ADA)
ENST00000696075.1:c.*589A>G (ADA) ENSP00000512374.1:n.*589A>G
ENST00000696076.1:c.688A>G (ADA) ENSP00000512375.1:p.Ser230Gly
ENST00000696077.1:c.613A>G (ADA) ENSP00000512376.1:p.Ser205Gly
ENST00000696078.1:c.616A>G (ADA) ENSP00000512377.1:p.Ser206Gly
ENST00000696079.1:c.616A>G (ADA) ENSP00000512378.1:p.Ser206Gly
ENST00000696080.1:c.619A>G (ADA) ENSP00000512379.1:p.Ser207Gly
ENST00000696081.1:n.738A>G (ADA)
ENST00000696082.1:c.694A>G (ADA) ENSP00000512380.1:p.Ser232Gly
ENST00000696083.1:n.1500A>G (ADA)
ENST00000696084.1:n.720A>G (ADA)
ENST00000696104.1:c.363-136A>G (ADA) ENSP00000512399.1:n.363-136A>G
ENST00000696105.1:c.*160A>G (ADA) ENSP00000512400.1:n.*160A>G
ENST00000372874.9:c.619A>G (ADA) MANE Select ENSP00000361965.4:p.Ser207Gly
ENST00000372874.8:c.619A>G (ADA) ENSP00000361965.4:p.Ser207Gly
ENST00000372887.5:c.152-867T>C (PKIG) ENSP00000361978.1:n.152-867T>C
ENST00000464097.5:n.293A>G (ADA)
ENST00000492931.5:n.703A>G (ADA)
ENST00000536532.5:c.619A>G (ADA) ENSP00000440946.1:p.Ser207Gly
ENST00000537820.1:c.607-136A>G (ADA) ENSP00000441818.1:n.607-136A>G
ENST00000539235.5:c.*3A>G (ADA) ENSP00000446464.1:n.*3A>G
NM_000022.2:c.619A>G , LRG_16t1:c.619A>G (ADA) NP_000013.2:p.Ser207Gly
XM_005260236.2:c.607-136A>G (ADA) XP_005260293.1:n.607-136A>G
XM_011528478.1:c.214A>G (ADA) XP_011526780.1:p.Ser72Gly
XM_011528479.1:c.214A>G (ADA) XP_011526781.1:p.Ser72Gly
XR_244129.1:n.673A>G (ADA)
NM_000022.3:c.619A>G (ADA) NP_000013.2:p.Ser207Gly
NM_001322050.1:c.214A>G (ADA) NP_001308979.1:p.Ser72Gly
NM_001322051.1:c.607-136A>G (ADA) NP_001308980.1:n.607-136A>G
NR_136160.1:n.770A>G (ADA)
NM_000022.4:c.619A>G (ADA) MANE Select NP_000013.2:p.Ser207Gly
NM_001322050.2:c.214A>G (ADA) NP_001308979.1:p.Ser72Gly
NM_001322051.2:c.607-136A>G (ADA) NP_001308980.1:n.607-136A>G
NR_136160.2:n.711A>G (ADA)