Canonical Allele Identifier: CA510593643

Linked Data

MyVariant Identifiers: chr20:g.43252864A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624223A>C , CM000682.2:g.44624223A>C GRCh38
NC_000020.10:g.43252864A>C , CM000682.1:g.43252864A>C GRCh37
NC_000020.9:g.42686278A>C NCBI36
NG_007385.1:g.32513T>G , LRG_16:g.32513T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.676T>G (ADA)
ENST00000536076.2:c.432T>G (ADA) ENSP00000512234.1:p.Pro144=
ENST00000536532.6:c.585T>G (ADA) ENSP00000440946.1:p.Pro195=
ENST00000537820.2:c.585T>G (ADA) ENSP00000441818.1:p.Pro195=
ENST00000539235.6:c.219-1145T>G (ADA) ENSP00000446464.1:n.219-1145T>G
ENST00000695889.1:c.219-1293T>G (ADA) ENSP00000512240.1:n.219-1293T>G
ENST00000695890.1:n.2388T>G (ADA)
ENST00000695891.1:c.219-1293T>G (ADA) ENSP00000512241.1:n.219-1293T>G
ENST00000695927.1:c.663T>G (ADA) ENSP00000512270.1:p.Pro221=
ENST00000695949.1:c.582T>G (ADA) ENSP00000512281.1:p.Pro194=
ENST00000695957.1:c.*76T>G (ADA) ENSP00000512286.1:n.*76T>G
ENST00000695991.1:c.217-1293T>G (ADA) ENSP00000512314.1:n.217-1293T>G
ENST00000695992.1:c.585T>G (ADA) ENSP00000512315.1:p.Pro195=
ENST00000695993.1:c.585T>G (ADA) ENSP00000512316.1:p.Pro195=
ENST00000695994.1:c.585T>G (ADA) ENSP00000512317.1:p.Pro195=
ENST00000695995.1:c.217-1145T>G (ADA) ENSP00000512318.1:n.217-1145T>G
ENST00000695996.1:n.656T>G (ADA)
ENST00000695997.1:n.540T>G (ADA)
ENST00000696003.1:n.677T>G (ADA)
ENST00000696004.1:n.677T>G (ADA)
ENST00000696005.1:c.107T>G (ADA)
ENST00000696006.1:c.585T>G (ADA) ENSP00000512325.1:p.Pro195=
ENST00000696007.1:c.436T>G (ADA) ENSP00000512326.1:n.436T>G
ENST00000696008.1:n.1740T>G (ADA)
ENST00000696009.1:n.1935T>G (ADA)
ENST00000696017.1:c.582T>G (ADA) ENSP00000512333.1:p.Pro194=
ENST00000696034.1:c.585T>G (ADA) ENSP00000512343.1:p.Pro195=
ENST00000696035.1:n.695T>G (ADA)
ENST00000696036.1:n.1275T>G (ADA)
ENST00000696037.1:n.2262T>G (ADA)
ENST00000696038.1:c.*331T>G (ADA) ENSP00000512344.1:n.*331T>G
ENST00000696039.1:n.873T>G (ADA)
ENST00000696058.1:c.585T>G (ADA) ENSP00000512361.1:p.Pro195=
ENST00000696059.1:c.*530T>G (ADA) ENSP00000512362.1:n.*530T>G
ENST00000696060.1:c.585T>G (ADA) ENSP00000512363.1:p.Pro195=
ENST00000696061.1:c.582T>G (ADA) ENSP00000512364.1:p.Pro194=
ENST00000696062.1:c.648T>G (ADA) ENSP00000512365.1:p.Pro216=
ENST00000696063.1:c.660T>G (ADA) ENSP00000512366.1:p.Pro220=
ENST00000696064.1:c.432T>G (ADA) ENSP00000512367.1:p.Pro144=
ENST00000696065.1:c.66-1293T>G (ADA) ENSP00000512368.1:n.66-1293T>G
ENST00000696074.1:n.201T>G (ADA)
ENST00000696075.1:c.*555T>G (ADA) ENSP00000512374.1:n.*555T>G
ENST00000696076.1:c.585T>G (ADA) ENSP00000512375.1:p.Pro195=
ENST00000696077.1:c.582T>G (ADA) ENSP00000512376.1:p.Pro194=
ENST00000696078.1:c.585T>G (ADA) ENSP00000512377.1:p.Pro195=
ENST00000696079.1:c.585T>G (ADA) ENSP00000512378.1:p.Pro195=
ENST00000696080.1:c.585T>G (ADA) ENSP00000512379.1:p.Pro195=
ENST00000696081.1:n.704T>G (ADA)
ENST00000696082.1:c.663T>G (ADA) ENSP00000512380.1:p.Pro221=
ENST00000696083.1:n.1466T>G (ADA)
ENST00000696084.1:n.686T>G (ADA)
ENST00000696104.1:c.363-1293T>G (ADA) ENSP00000512399.1:n.363-1293T>G
ENST00000696105.1:c.*126T>G (ADA) ENSP00000512400.1:n.*126T>G
ENST00000372874.9:c.585T>G (ADA) MANE Select ENSP00000361965.4:p.Pro195=
ENST00000372874.8:c.585T>G (ADA) ENSP00000361965.4:p.Pro195=
ENST00000372887.5:c.*247A>C (PKIG) ENSP00000361978.1:n.*247A>C
ENST00000464097.5:n.259T>G (ADA)
ENST00000492931.5:n.669T>G (ADA)
ENST00000536532.5:c.585T>G (ADA) ENSP00000440946.1:p.Pro195=
ENST00000537820.1:c.585T>G (ADA) ENSP00000441818.1:p.Pro195=
ENST00000539235.5:c.219-1145T>G (ADA) ENSP00000446464.1:n.219-1145T>G
NM_000022.2:c.585T>G , LRG_16t1:c.585T>G (ADA) NP_000013.2:p.Pro195=
XM_005260236.2:c.585T>G (ADA) XP_005260293.1:p.Pro195=
XM_011528478.1:c.180T>G (ADA) XP_011526780.1:p.Pro60=
XM_011528479.1:c.180T>G (ADA) XP_011526781.1:p.Pro60=
XR_244129.1:n.639T>G (ADA)
NM_000022.3:c.585T>G (ADA) NP_000013.2:p.Pro195=
NM_001322050.1:c.180T>G (ADA) NP_001308979.1:p.Pro60=
NM_001322051.1:c.585T>G (ADA) NP_001308980.1:p.Pro195=
NR_136160.1:n.736T>G (ADA)
NM_000022.4:c.585T>G (ADA) MANE Select NP_000013.2:p.Pro195=
NM_001322050.2:c.180T>G (ADA) NP_001308979.1:p.Pro60=
NM_001322051.2:c.585T>G (ADA) NP_001308980.1:p.Pro195=
NR_136160.2:n.677T>G (ADA)