Canonical Allele Identifier: CA2652990467

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44622961G>C , CM000682.2:g.44622961G>C GRCh38
NC_000020.10:g.43251602G>C , CM000682.1:g.43251602G>C GRCh37
NC_000020.9:g.42685016G>C NCBI36
NG_007385.1:g.33775C>G , LRG_16:g.33775C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.815C>G (ADA)
ENST00000536076.2:c.526-31C>G (ADA) ENSP00000512234.1:n.526-31C>G
ENST00000536532.6:c.679-31C>G (ADA) ENSP00000440946.1:n.679-31C>G
ENST00000537820.2:c.607-31C>G (ADA) ENSP00000441818.1:n.607-31C>G
ENST00000539235.6:c.*63-31C>G (ADA) ENSP00000446464.1:n.*63-31C>G
ENST00000695889.1:c.219-31C>G (ADA) ENSP00000512240.1:n.219-31C>G
ENST00000695890.1:n.2527C>G (ADA)
ENST00000695891.1:c.219-31C>G (ADA) ENSP00000512241.1:n.219-31C>G
ENST00000695927.1:c.757-31C>G (ADA) ENSP00000512270.1:n.757-31C>G
ENST00000695949.1:c.604-31C>G (ADA) ENSP00000512281.1:n.604-31C>G
ENST00000695957.1:c.*170-31C>G (ADA) ENSP00000512286.1:n.*170-31C>G
ENST00000695991.1:c.217-31C>G (ADA) ENSP00000512314.1:n.217-31C>G
ENST00000695992.1:c.679-31C>G (ADA) ENSP00000512315.1:n.679-31C>G
ENST00000695993.1:c.679-31C>G (ADA) ENSP00000512316.1:n.679-31C>G
ENST00000695994.1:c.652-31C>G (ADA) ENSP00000512317.1:n.652-31C>G
ENST00000695995.1:c.289-31C>G (ADA) ENSP00000512318.1:n.289-31C>G
ENST00000695996.1:n.795C>G (ADA)
ENST00000696003.1:n.816C>G (ADA)
ENST00000696004.1:n.816C>G (ADA)
ENST00000696005.1:c.129-31C>G (ADA)
ENST00000696006.1:c.607-31C>G (ADA) ENSP00000512325.1:n.607-31C>G
ENST00000696007.1:c.575C>G (ADA) ENSP00000512326.1:n.575C>G
ENST00000696008.1:n.3002C>G (ADA)
ENST00000696017.1:c.676-31C>G (ADA) ENSP00000512333.1:n.676-31C>G
ENST00000696034.1:c.679-31C>G (ADA) ENSP00000512343.1:n.679-31C>G
ENST00000696035.1:n.834C>G (ADA)
ENST00000696036.1:n.1414C>G (ADA)
ENST00000696037.1:n.2356-31C>G (ADA)
ENST00000696038.1:c.*470C>G (ADA) ENSP00000512344.1:n.*470C>G
ENST00000696039.1:n.1012C>G (ADA)
ENST00000696058.1:c.676-31C>G (ADA) ENSP00000512361.1:n.676-31C>G
ENST00000696059.1:c.*624-31C>G (ADA) ENSP00000512362.1:n.*624-31C>G
ENST00000696060.1:c.748-31C>G (ADA) ENSP00000512363.1:n.748-31C>G
ENST00000696061.1:c.676-31C>G (ADA) ENSP00000512364.1:n.676-31C>G
ENST00000696062.1:c.742-31C>G (ADA) ENSP00000512365.1:n.742-31C>G
ENST00000696063.1:c.754-31C>G (ADA) ENSP00000512366.1:n.754-31C>G
ENST00000696064.1:c.526-31C>G (ADA) ENSP00000512367.1:n.526-31C>G
ENST00000696065.1:c.66-31C>G (ADA) ENSP00000512368.1:n.66-31C>G
ENST00000696073.1:n.959C>G (ADA)
ENST00000696074.1:n.295-31C>G (ADA)
ENST00000696075.1:c.*649-31C>G (ADA) ENSP00000512374.1:n.*649-31C>G
ENST00000696076.1:c.748-31C>G (ADA) ENSP00000512375.1:n.748-31C>G
ENST00000696077.1:c.673-31C>G (ADA) ENSP00000512376.1:n.673-31C>G
ENST00000696078.1:c.676-31C>G (ADA) ENSP00000512377.1:n.676-31C>G
ENST00000696079.1:c.676-31C>G (ADA) ENSP00000512378.1:n.676-31C>G
ENST00000696080.1:c.679-31C>G (ADA) ENSP00000512379.1:n.679-31C>G
ENST00000696081.1:n.798-31C>G (ADA)
ENST00000696082.1:c.754-31C>G (ADA) ENSP00000512380.1:n.754-31C>G
ENST00000696083.1:n.1605C>G (ADA)
ENST00000696084.1:n.825C>G (ADA)
ENST00000696104.1:c.363-31C>G (ADA) ENSP00000512399.1:n.363-31C>G
ENST00000372874.9:c.679-31C>G (ADA) MANE Select ENSP00000361965.4:n.679-31C>G
ENST00000372874.8:c.679-31C>G (ADA) ENSP00000361965.4:n.679-31C>G
ENST00000372887.5:c.152-972G>C (PKIG) ENSP00000361978.1:n.152-972G>C
ENST00000464097.5:n.398C>G (ADA)
ENST00000492931.5:n.808C>G (ADA)
ENST00000536532.5:c.679-31C>G (ADA) ENSP00000440946.1:n.679-31C>G
ENST00000537820.1:c.607-31C>G (ADA) ENSP00000441818.1:n.607-31C>G
ENST00000539235.5:c.*63-31C>G (ADA) ENSP00000446464.1:n.*63-31C>G
NM_000022.2:c.679-31C>G , LRG_16t1:c.679-31C>G (ADA) NP_000013.2:n.679-31C>G
XM_005260236.2:c.607-31C>G (ADA) XP_005260293.1:n.607-31C>G
XM_011528478.1:c.274-31C>G (ADA) XP_011526780.1:n.274-31C>G
XM_011528479.1:c.274-31C>G (ADA) XP_011526781.1:n.274-31C>G
XR_244129.1:n.733-31C>G (ADA)
NM_000022.3:c.679-31C>G (ADA) NP_000013.2:n.679-31C>G
NM_001322050.1:c.274-31C>G (ADA) NP_001308979.1:n.274-31C>G
NM_001322051.1:c.607-31C>G (ADA) NP_001308980.1:n.607-31C>G
NR_136160.1:n.830-31C>G (ADA)
NM_000022.4:c.679-31C>G (ADA) MANE Select NP_000013.2:n.679-31C>G
NM_001322050.2:c.274-31C>G (ADA) NP_001308979.1:n.274-31C>G
NM_001322051.2:c.607-31C>G (ADA) NP_001308980.1:n.607-31C>G
NR_136160.2:n.771-31C>G (ADA)