Canonical Allele Identifier: CA2365854633

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620390C= , CM000682.2:g.44620390C= GRCh38
NC_000020.10:g.43249031C= , CM000682.1:g.43249031C= GRCh37
NC_000020.9:g.42682445C= NCBI36
NG_007385.1:g.36346G= , LRG_16:g.36346G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.1154G= (ADA)
ENST00000536076.2:c.834G= (ADA) ENSP00000512234.1:p.Ala278=
ENST00000536532.6:c.*130G= (ADA) ENSP00000440946.1:n.*130G=
ENST00000537820.2:c.915G= (ADA) ENSP00000441818.1:p.Ala305=
ENST00000539235.6:c.*371G= (ADA) ENSP00000446464.1:n.*371G=
ENST00000695889.1:c.462G= (ADA) ENSP00000512240.1:p.Ala154=
ENST00000695890.1:n.5098G= (ADA)
ENST00000695891.1:c.527G= (ADA) ENSP00000512241.1:n.527G=
ENST00000695927.1:c.1065G= (ADA) ENSP00000512270.1:p.Ala355=
ENST00000695949.1:c.912G= (ADA) ENSP00000512281.1:p.Ala304=
ENST00000695956.1:c.142G= (ADA)
ENST00000695957.1:c.*478G= (ADA) ENSP00000512286.1:n.*478G=
ENST00000695991.1:c.525G= (ADA) ENSP00000512314.1:p.Ala175=
ENST00000695992.1:c.*130G= (ADA) ENSP00000512315.1:n.*130G=
ENST00000695993.1:c.987G= (ADA) ENSP00000512316.1:p.Ala329=
ENST00000695994.1:c.*130G= (ADA) ENSP00000512317.1:n.*130G=
ENST00000695995.1:c.597G= (ADA) ENSP00000512318.1:p.Ala199=
ENST00000695996.1:n.1069G= (ADA)
ENST00000696003.1:n.2771G= (ADA)
ENST00000696004.1:n.1771G= (ADA)
ENST00000696005.1:c.437G= (ADA)
ENST00000696006.1:c.*130G= (ADA) ENSP00000512325.1:n.*130G=
ENST00000696007.1:c.914G= (ADA) ENSP00000512326.1:n.914G=
ENST00000696008.1:n.3341G= (ADA)
ENST00000696017.1:c.984G= (ADA) ENSP00000512333.1:p.Ala328=
ENST00000696034.1:c.*130G= (ADA) ENSP00000512343.1:n.*130G=
ENST00000696035.1:n.1173G= (ADA)
ENST00000696036.1:n.1688G= (ADA)
ENST00000696037.1:n.2664G= (ADA)
ENST00000696038.1:c.*744G= (ADA) ENSP00000512344.1:n.*744G=
ENST00000696039.1:n.1351G= (ADA)
ENST00000696058.1:c.984G= (ADA) ENSP00000512361.1:p.Ala328=
ENST00000696059.1:c.*932G= (ADA) ENSP00000512362.1:n.*932G=
ENST00000696060.1:c.1056G= (ADA) ENSP00000512363.1:p.Ala352=
ENST00000696061.1:c.984G= (ADA) ENSP00000512364.1:p.Ala328=
ENST00000696062.1:c.1050G= (ADA) ENSP00000512365.1:p.Ala350=
ENST00000696063.1:c.1062G= (ADA) ENSP00000512366.1:p.Ala354=
ENST00000696064.1:c.834G= (ADA) ENSP00000512367.1:p.Ala278=
ENST00000696065.1:c.309G= (ADA) ENSP00000512368.1:p.Ala103=
ENST00000696072.1:n.342G= (ADA)
ENST00000696073.1:n.1298G= (ADA)
ENST00000696074.1:n.538G= (ADA)
ENST00000696075.1:c.*957G= (ADA) ENSP00000512374.1:n.*957G=
ENST00000696076.1:c.1056G= (ADA) ENSP00000512375.1:p.Ala352=
ENST00000696077.1:c.981G= (ADA) ENSP00000512376.1:p.Ala327=
ENST00000696078.1:c.984G= (ADA) ENSP00000512377.1:p.Ala328=
ENST00000696079.1:c.984G= (ADA) ENSP00000512378.1:p.Ala328=
ENST00000696080.1:c.987G= (ADA) ENSP00000512379.1:p.Ala329=
ENST00000696081.1:n.1106G= (ADA)
ENST00000696082.1:c.1062G= (ADA) ENSP00000512380.1:p.Ala354=
ENST00000696083.1:n.1944G= (ADA)
ENST00000696084.1:n.1164G= (ADA)
ENST00000696104.1:c.*56G= (ADA) ENSP00000512399.1:n.*56G=
ENST00000372874.9:c.987G= (ADA) MANE Select ENSP00000361965.4:p.Ala329=
ENST00000372874.8:c.987G= (ADA) ENSP00000361965.4:p.Ala329=
ENST00000372887.5:c.152-3543C= (PKIG) ENSP00000361978.1:n.152-3543C=
ENST00000464097.5:n.1353G= (ADA)
ENST00000492931.5:n.1147G= (ADA)
ENST00000536532.5:c.*130G= (ADA) ENSP00000440946.1:n.*130G=
ENST00000537820.1:c.915G= (ADA) ENSP00000441818.1:p.Ala305=
ENST00000539235.5:c.*371G= (ADA) ENSP00000446464.1:n.*371G=
NM_000022.2:c.987G= , LRG_16t1:c.987G= (ADA) NP_000013.2:p.Ala329=
XM_005260236.2:c.915G= (ADA) XP_005260293.1:p.Ala305=
XM_011528478.1:c.582G= (ADA) XP_011526780.1:p.Ala194=
XM_011528479.1:c.582G= (ADA) XP_011526781.1:p.Ala194=
XR_244129.1:n.976G= (ADA)
NM_000022.3:c.987G= (ADA) NP_000013.2:p.Ala329=
NM_001322050.1:c.582G= (ADA) NP_001308979.1:p.Ala194=
NM_001322051.1:c.915G= (ADA) NP_001308980.1:p.Ala305=
NR_136160.1:n.1073G= (ADA)
NM_000022.4:c.987G= (ADA) MANE Select NP_000013.2:p.Ala329=
NM_001322050.2:c.582G= (ADA) NP_001308979.1:p.Ala194=
NM_001322051.2:c.915G= (ADA) NP_001308980.1:p.Ala305=
NR_136160.2:n.1014G= (ADA)