Canonical Allele Identifier: CA409118669

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620394T>A , CM000682.2:g.44620394T>A GRCh38
NC_000020.10:g.43249035T>A , CM000682.1:g.43249035T>A GRCh37
NC_000020.9:g.42682449T>A NCBI36
NG_007385.1:g.36342A>T , LRG_16:g.36342A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.1150A>T (ADA)
ENST00000536076.2:c.830A>T (ADA) ENSP00000512234.1:p.Asn277Ile
ENST00000536532.6:c.*126A>T (ADA) ENSP00000440946.1:n.*126A>T
ENST00000537820.2:c.911A>T (ADA) ENSP00000441818.1:p.Asn304Ile
ENST00000539235.6:c.*367A>T (ADA) ENSP00000446464.1:n.*367A>T
ENST00000695889.1:c.458A>T (ADA) ENSP00000512240.1:p.Asn153Ile
ENST00000695890.1:n.5094A>T (ADA)
ENST00000695891.1:c.523A>T (ADA) ENSP00000512241.1:n.523A>T
ENST00000695927.1:c.1061A>T (ADA) ENSP00000512270.1:p.Asn354Ile
ENST00000695949.1:c.908A>T (ADA) ENSP00000512281.1:p.Asn303Ile
ENST00000695956.1:c.138A>T (ADA)
ENST00000695957.1:c.*474A>T (ADA) ENSP00000512286.1:n.*474A>T
ENST00000695991.1:c.521A>T (ADA) ENSP00000512314.1:p.Asn174Ile
ENST00000695992.1:c.*126A>T (ADA) ENSP00000512315.1:n.*126A>T
ENST00000695993.1:c.983A>T (ADA) ENSP00000512316.1:p.Asn328Ile
ENST00000695994.1:c.*126A>T (ADA) ENSP00000512317.1:n.*126A>T
ENST00000695995.1:c.593A>T (ADA) ENSP00000512318.1:p.Asn198Ile
ENST00000695996.1:n.1065A>T (ADA)
ENST00000696003.1:n.2767A>T (ADA)
ENST00000696004.1:n.1767A>T (ADA)
ENST00000696005.1:c.433A>T (ADA)
ENST00000696006.1:c.*126A>T (ADA) ENSP00000512325.1:n.*126A>T
ENST00000696007.1:c.910A>T (ADA) ENSP00000512326.1:n.910A>T
ENST00000696008.1:n.3337A>T (ADA)
ENST00000696017.1:c.980A>T (ADA) ENSP00000512333.1:p.Asn327Ile
ENST00000696034.1:c.*126A>T (ADA) ENSP00000512343.1:n.*126A>T
ENST00000696035.1:n.1169A>T (ADA)
ENST00000696036.1:n.1684A>T (ADA)
ENST00000696037.1:n.2660A>T (ADA)
ENST00000696038.1:c.*740A>T (ADA) ENSP00000512344.1:n.*740A>T
ENST00000696039.1:n.1347A>T (ADA)
ENST00000696058.1:c.980A>T (ADA) ENSP00000512361.1:p.Asn327Ile
ENST00000696059.1:c.*928A>T (ADA) ENSP00000512362.1:n.*928A>T
ENST00000696060.1:c.1052A>T (ADA) ENSP00000512363.1:p.Asn351Ile
ENST00000696061.1:c.980A>T (ADA) ENSP00000512364.1:p.Asn327Ile
ENST00000696062.1:c.1046A>T (ADA) ENSP00000512365.1:p.Asn349Ile
ENST00000696063.1:c.1058A>T (ADA) ENSP00000512366.1:p.Asn353Ile
ENST00000696064.1:c.830A>T (ADA) ENSP00000512367.1:p.Asn277Ile
ENST00000696065.1:c.305A>T (ADA) ENSP00000512368.1:p.Asn102Ile
ENST00000696072.1:n.338A>T (ADA)
ENST00000696073.1:n.1294A>T (ADA)
ENST00000696074.1:n.534A>T (ADA)
ENST00000696075.1:c.*953A>T (ADA) ENSP00000512374.1:n.*953A>T
ENST00000696076.1:c.1052A>T (ADA) ENSP00000512375.1:p.Asn351Ile
ENST00000696077.1:c.977A>T (ADA) ENSP00000512376.1:p.Asn326Ile
ENST00000696078.1:c.980A>T (ADA) ENSP00000512377.1:p.Asn327Ile
ENST00000696079.1:c.980A>T (ADA) ENSP00000512378.1:p.Asn327Ile
ENST00000696080.1:c.983A>T (ADA) ENSP00000512379.1:p.Asn328Ile
ENST00000696081.1:n.1102A>T (ADA)
ENST00000696082.1:c.1058A>T (ADA) ENSP00000512380.1:p.Asn353Ile
ENST00000696083.1:n.1940A>T (ADA)
ENST00000696084.1:n.1160A>T (ADA)
ENST00000696104.1:c.*52A>T (ADA) ENSP00000512399.1:n.*52A>T
ENST00000372874.9:c.983A>T (ADA) MANE Select ENSP00000361965.4:p.Asn328Ile
ENST00000372874.8:c.983A>T (ADA) ENSP00000361965.4:p.Asn328Ile
ENST00000372887.5:c.152-3539T>A (PKIG) ENSP00000361978.1:n.152-3539T>A
ENST00000464097.5:n.1349A>T (ADA)
ENST00000492931.5:n.1143A>T (ADA)
ENST00000536532.5:c.*126A>T (ADA) ENSP00000440946.1:n.*126A>T
ENST00000537820.1:c.911A>T (ADA) ENSP00000441818.1:p.Asn304Ile
ENST00000539235.5:c.*367A>T (ADA) ENSP00000446464.1:n.*367A>T
NM_000022.2:c.983A>T , LRG_16t1:c.983A>T (ADA) NP_000013.2:p.Asn328Ile
XM_005260236.2:c.911A>T (ADA) XP_005260293.1:p.Asn304Ile
XM_011528478.1:c.578A>T (ADA) XP_011526780.1:p.Asn193Ile
XM_011528479.1:c.578A>T (ADA) XP_011526781.1:p.Asn193Ile
XR_244129.1:n.972A>T (ADA)
NM_000022.3:c.983A>T (ADA) NP_000013.2:p.Asn328Ile
NM_001322050.1:c.578A>T (ADA) NP_001308979.1:p.Asn193Ile
NM_001322051.1:c.911A>T (ADA) NP_001308980.1:p.Asn304Ile
NR_136160.1:n.1069A>T (ADA)
NM_000022.4:c.983A>T (ADA) MANE Select NP_000013.2:p.Asn328Ile
NM_001322050.2:c.578A>T (ADA) NP_001308979.1:p.Asn193Ile
NM_001322051.2:c.911A>T (ADA) NP_001308980.1:p.Asn304Ile
NR_136160.2:n.1010A>T (ADA)