Canonical Allele Identifier: CA409120429

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623035T>A , CM000682.2:g.44623035T>A GRCh38
NC_000020.10:g.43251676T>A , CM000682.1:g.43251676T>A GRCh37
NC_000020.9:g.42685090T>A NCBI36
NG_007385.1:g.33701A>T , LRG_16:g.33701A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.741A>T (ADA)
ENST00000536076.2:c.497A>T (ADA) ENSP00000512234.1:p.Glu166Val
ENST00000536532.6:c.650A>T (ADA) ENSP00000440946.1:p.Glu217Val
ENST00000537820.2:c.607-105A>T (ADA) ENSP00000441818.1:n.607-105A>T
ENST00000539235.6:c.*34A>T (ADA) ENSP00000446464.1:n.*34A>T
ENST00000695889.1:c.219-105A>T (ADA) ENSP00000512240.1:n.219-105A>T
ENST00000695890.1:n.2453A>T (ADA)
ENST00000695891.1:c.219-105A>T (ADA) ENSP00000512241.1:n.219-105A>T
ENST00000695927.1:c.728A>T (ADA) ENSP00000512270.1:p.Glu243Val
ENST00000695949.1:c.604-105A>T (ADA) ENSP00000512281.1:n.604-105A>T
ENST00000695957.1:c.*141A>T (ADA) ENSP00000512286.1:n.*141A>T
ENST00000695991.1:c.217-105A>T (ADA) ENSP00000512314.1:n.217-105A>T
ENST00000695992.1:c.650A>T (ADA) ENSP00000512315.1:p.Glu217Val
ENST00000695993.1:c.650A>T (ADA) ENSP00000512316.1:p.Glu217Val
ENST00000695994.1:c.650A>T (ADA) ENSP00000512317.1:p.Glu217Val
ENST00000695995.1:c.260A>T (ADA) ENSP00000512318.1:p.Glu87Val
ENST00000695996.1:n.721A>T (ADA)
ENST00000696003.1:n.742A>T (ADA)
ENST00000696004.1:n.742A>T (ADA)
ENST00000696005.1:c.129-105A>T (ADA)
ENST00000696006.1:c.607-105A>T (ADA) ENSP00000512325.1:n.607-105A>T
ENST00000696007.1:c.501A>T (ADA) ENSP00000512326.1:n.501A>T
ENST00000696008.1:n.2928A>T (ADA)
ENST00000696017.1:c.647A>T (ADA) ENSP00000512333.1:p.Glu216Val
ENST00000696034.1:c.650A>T (ADA) ENSP00000512343.1:p.Glu217Val
ENST00000696035.1:n.760A>T (ADA)
ENST00000696036.1:n.1340A>T (ADA)
ENST00000696037.1:n.2327A>T (ADA)
ENST00000696038.1:c.*396A>T (ADA) ENSP00000512344.1:n.*396A>T
ENST00000696039.1:n.938A>T (ADA)
ENST00000696058.1:c.647A>T (ADA) ENSP00000512361.1:p.Glu216Val
ENST00000696059.1:c.*595A>T (ADA) ENSP00000512362.1:n.*595A>T
ENST00000696060.1:c.719A>T (ADA) ENSP00000512363.1:p.Glu240Val
ENST00000696061.1:c.647A>T (ADA) ENSP00000512364.1:p.Glu216Val
ENST00000696062.1:c.713A>T (ADA) ENSP00000512365.1:p.Glu238Val
ENST00000696063.1:c.725A>T (ADA) ENSP00000512366.1:p.Glu242Val
ENST00000696064.1:c.497A>T (ADA) ENSP00000512367.1:p.Glu166Val
ENST00000696065.1:c.66-105A>T (ADA) ENSP00000512368.1:n.66-105A>T
ENST00000696073.1:n.885A>T (ADA)
ENST00000696074.1:n.266A>T (ADA)
ENST00000696075.1:c.*620A>T (ADA) ENSP00000512374.1:n.*620A>T
ENST00000696076.1:c.719A>T (ADA) ENSP00000512375.1:p.Glu240Val
ENST00000696077.1:c.644A>T (ADA) ENSP00000512376.1:p.Glu215Val
ENST00000696078.1:c.647A>T (ADA) ENSP00000512377.1:p.Glu216Val
ENST00000696079.1:c.647A>T (ADA) ENSP00000512378.1:p.Glu216Val
ENST00000696080.1:c.650A>T (ADA) ENSP00000512379.1:p.Glu217Val
ENST00000696081.1:n.769A>T (ADA)
ENST00000696082.1:c.725A>T (ADA) ENSP00000512380.1:p.Glu242Val
ENST00000696083.1:n.1531A>T (ADA)
ENST00000696084.1:n.751A>T (ADA)
ENST00000696104.1:c.363-105A>T (ADA) ENSP00000512399.1:n.363-105A>T
ENST00000696105.1:c.*191A>T (ADA) ENSP00000512400.1:n.*191A>T
ENST00000372874.9:c.650A>T (ADA) MANE Select ENSP00000361965.4:p.Glu217Val
ENST00000372874.8:c.650A>T (ADA) ENSP00000361965.4:p.Glu217Val
ENST00000372887.5:c.152-898T>A (PKIG) ENSP00000361978.1:n.152-898T>A
ENST00000464097.5:n.324A>T (ADA)
ENST00000492931.5:n.734A>T (ADA)
ENST00000536532.5:c.650A>T (ADA) ENSP00000440946.1:p.Glu217Val
ENST00000537820.1:c.607-105A>T (ADA) ENSP00000441818.1:n.607-105A>T
ENST00000539235.5:c.*34A>T (ADA) ENSP00000446464.1:n.*34A>T
NM_000022.2:c.650A>T , LRG_16t1:c.650A>T (ADA) NP_000013.2:p.Glu217Val
XM_005260236.2:c.607-105A>T (ADA) XP_005260293.1:n.607-105A>T
XM_011528478.1:c.245A>T (ADA) XP_011526780.1:p.Glu82Val
XM_011528479.1:c.245A>T (ADA) XP_011526781.1:p.Glu82Val
XR_244129.1:n.704A>T (ADA)
NM_000022.3:c.650A>T (ADA) NP_000013.2:p.Glu217Val
NM_001322050.1:c.245A>T (ADA) NP_001308979.1:p.Glu82Val
NM_001322051.1:c.607-105A>T (ADA) NP_001308980.1:n.607-105A>T
NR_136160.1:n.801A>T (ADA)
NM_000022.4:c.650A>T (ADA) MANE Select NP_000013.2:p.Glu217Val
NM_001322050.2:c.245A>T (ADA) NP_001308979.1:p.Glu82Val
NM_001322051.2:c.607-105A>T (ADA) NP_001308980.1:n.607-105A>T
NR_136160.2:n.742A>T (ADA)