Canonical Allele Identifier: CA2365856020

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623164A= , CM000682.2:g.44623164A= GRCh38
NC_000020.10:g.43251805A= , CM000682.1:g.43251805A= GRCh37
NC_000020.9:g.42685219A= NCBI36
NG_007385.1:g.33572T= , LRG_16:g.33572T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.698-86T= (ADA)
ENST00000536076.2:c.454-86T= (ADA) ENSP00000512234.1:n.454-86T=
ENST00000536532.6:c.607-86T= (ADA) ENSP00000440946.1:n.607-86T=
ENST00000537820.2:c.607-234T= (ADA) ENSP00000441818.1:n.607-234T=
ENST00000539235.6:c.219-86T= (ADA) ENSP00000446464.1:n.219-86T=
ENST00000695889.1:c.219-234T= (ADA) ENSP00000512240.1:n.219-234T=
ENST00000695890.1:n.2410-86T= (ADA)
ENST00000695891.1:c.219-234T= (ADA) ENSP00000512241.1:n.219-234T=
ENST00000695927.1:c.685-86T= (ADA) ENSP00000512270.1:n.685-86T=
ENST00000695949.1:c.604-234T= (ADA) ENSP00000512281.1:n.604-234T=
ENST00000695957.1:c.*98-86T= (ADA) ENSP00000512286.1:n.*98-86T=
ENST00000695991.1:c.217-234T= (ADA) ENSP00000512314.1:n.217-234T=
ENST00000695992.1:c.607-86T= (ADA) ENSP00000512315.1:n.607-86T=
ENST00000695993.1:c.607-86T= (ADA) ENSP00000512316.1:n.607-86T=
ENST00000695994.1:c.607-86T= (ADA) ENSP00000512317.1:n.607-86T=
ENST00000695995.1:c.217-86T= (ADA) ENSP00000512318.1:n.217-86T=
ENST00000695996.1:n.678-86T= (ADA)
ENST00000696003.1:n.699-86T= (ADA)
ENST00000696004.1:n.699-86T= (ADA)
ENST00000696005.1:c.129-234T= (ADA)
ENST00000696006.1:c.607-234T= (ADA) ENSP00000512325.1:n.607-234T=
ENST00000696007.1:c.458-86T= (ADA) ENSP00000512326.1:n.458-86T=
ENST00000696008.1:n.2799T= (ADA)
ENST00000696017.1:c.604-86T= (ADA) ENSP00000512333.1:n.604-86T=
ENST00000696034.1:c.607-86T= (ADA) ENSP00000512343.1:n.607-86T=
ENST00000696035.1:n.717-86T= (ADA)
ENST00000696036.1:n.1297-86T= (ADA)
ENST00000696037.1:n.2284-86T= (ADA)
ENST00000696038.1:c.*353-86T= (ADA) ENSP00000512344.1:n.*353-86T=
ENST00000696039.1:n.895-86T= (ADA)
ENST00000696058.1:c.607-89T= (ADA) ENSP00000512361.1:n.607-89T=
ENST00000696059.1:c.*552-86T= (ADA) ENSP00000512362.1:n.*552-86T=
ENST00000696060.1:c.607-17T= (ADA) ENSP00000512363.1:n.607-17T=
ENST00000696061.1:c.604-86T= (ADA) ENSP00000512364.1:n.604-86T=
ENST00000696062.1:c.670-86T= (ADA) ENSP00000512365.1:n.670-86T=
ENST00000696063.1:c.682-86T= (ADA) ENSP00000512366.1:n.682-86T=
ENST00000696064.1:c.454-86T= (ADA) ENSP00000512367.1:n.454-86T=
ENST00000696065.1:c.66-234T= (ADA) ENSP00000512368.1:n.66-234T=
ENST00000696073.1:n.756T= (ADA)
ENST00000696074.1:n.223-86T= (ADA)
ENST00000696075.1:c.*577-86T= (ADA) ENSP00000512374.1:n.*577-86T=
ENST00000696076.1:c.607-17T= (ADA) ENSP00000512375.1:n.607-17T=
ENST00000696077.1:c.604-89T= (ADA) ENSP00000512376.1:n.604-89T=
ENST00000696078.1:c.607-89T= (ADA) ENSP00000512377.1:n.607-89T=
ENST00000696079.1:c.607-89T= (ADA) ENSP00000512378.1:n.607-89T=
ENST00000696080.1:c.607-86T= (ADA) ENSP00000512379.1:n.607-86T=
ENST00000696081.1:n.726-86T= (ADA)
ENST00000696082.1:c.685-89T= (ADA) ENSP00000512380.1:n.685-89T=
ENST00000696083.1:n.1488-86T= (ADA)
ENST00000696084.1:n.708-86T= (ADA)
ENST00000696104.1:c.363-234T= (ADA) ENSP00000512399.1:n.363-234T=
ENST00000696105.1:c.*148-86T= (ADA) ENSP00000512400.1:n.*148-86T=
ENST00000372874.9:c.607-86T= (ADA) MANE Select ENSP00000361965.4:n.607-86T=
ENST00000372874.8:c.607-86T= (ADA) ENSP00000361965.4:n.607-86T=
ENST00000372887.5:c.152-769A= (PKIG) ENSP00000361978.1:n.152-769A=
ENST00000464097.5:n.281-86T= (ADA)
ENST00000492931.5:n.691-86T= (ADA)
ENST00000536532.5:c.607-86T= (ADA) ENSP00000440946.1:n.607-86T=
ENST00000537820.1:c.607-234T= (ADA) ENSP00000441818.1:n.607-234T=
ENST00000539235.5:c.219-86T= (ADA) ENSP00000446464.1:n.219-86T=
NM_000022.2:c.607-86T= , LRG_16t1:c.607-86T= (ADA) NP_000013.2:n.607-86T=
XM_005260236.2:c.607-234T= (ADA) XP_005260293.1:n.607-234T=
XM_011528478.1:c.202-86T= (ADA) XP_011526780.1:n.202-86T=
XM_011528479.1:c.202-86T= (ADA) XP_011526781.1:n.202-86T=
XR_244129.1:n.661-86T= (ADA)
NM_000022.3:c.607-86T= (ADA) NP_000013.2:n.607-86T=
NM_001322050.1:c.202-86T= (ADA) NP_001308979.1:n.202-86T=
NM_001322051.1:c.607-234T= (ADA) NP_001308980.1:n.607-234T=
NR_136160.1:n.758-86T= (ADA)
NM_000022.4:c.607-86T= (ADA) MANE Select NP_000013.2:n.607-86T=
NM_001322050.2:c.202-86T= (ADA) NP_001308979.1:n.202-86T=
NM_001322051.2:c.607-234T= (ADA) NP_001308980.1:n.607-234T=
NR_136160.2:n.699-86T= (ADA)