Canonical Allele Identifier: CA409118686

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44620401T>G , CM000682.2:g.44620401T>G GRCh38
NC_000020.10:g.43249042T>G , CM000682.1:g.43249042T>G GRCh37
NC_000020.9:g.42682456T>G NCBI36
NG_007385.1:g.36335A>C , LRG_16:g.36335A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.1143A>C (ADA)
ENST00000536076.2:c.823A>C (ADA) ENSP00000512234.1:p.Asn275His
ENST00000536532.6:c.*119A>C (ADA) ENSP00000440946.1:n.*119A>C
ENST00000537820.2:c.904A>C (ADA) ENSP00000441818.1:p.Asn302His
ENST00000539235.6:c.*360A>C (ADA) ENSP00000446464.1:n.*360A>C
ENST00000695889.1:c.451A>C (ADA) ENSP00000512240.1:p.Asn151His
ENST00000695890.1:n.5087A>C (ADA)
ENST00000695891.1:c.516A>C (ADA) ENSP00000512241.1:n.516A>C
ENST00000695927.1:c.1054A>C (ADA) ENSP00000512270.1:p.Asn352His
ENST00000695949.1:c.901A>C (ADA) ENSP00000512281.1:p.Asn301His
ENST00000695956.1:c.131A>C (ADA)
ENST00000695957.1:c.*467A>C (ADA) ENSP00000512286.1:n.*467A>C
ENST00000695991.1:c.514A>C (ADA) ENSP00000512314.1:p.Asn172His
ENST00000695992.1:c.*119A>C (ADA) ENSP00000512315.1:n.*119A>C
ENST00000695993.1:c.976A>C (ADA) ENSP00000512316.1:p.Asn326His
ENST00000695994.1:c.*119A>C (ADA) ENSP00000512317.1:n.*119A>C
ENST00000695995.1:c.586A>C (ADA) ENSP00000512318.1:p.Asn196His
ENST00000695996.1:n.1058A>C (ADA)
ENST00000696003.1:n.2760A>C (ADA)
ENST00000696004.1:n.1760A>C (ADA)
ENST00000696005.1:c.426A>C (ADA)
ENST00000696006.1:c.*119A>C (ADA) ENSP00000512325.1:n.*119A>C
ENST00000696007.1:c.903A>C (ADA) ENSP00000512326.1:n.903A>C
ENST00000696008.1:n.3330A>C (ADA)
ENST00000696017.1:c.973A>C (ADA) ENSP00000512333.1:p.Asn325His
ENST00000696034.1:c.*119A>C (ADA) ENSP00000512343.1:n.*119A>C
ENST00000696035.1:n.1162A>C (ADA)
ENST00000696036.1:n.1677A>C (ADA)
ENST00000696037.1:n.2653A>C (ADA)
ENST00000696038.1:c.*733A>C (ADA) ENSP00000512344.1:n.*733A>C
ENST00000696039.1:n.1340A>C (ADA)
ENST00000696058.1:c.973A>C (ADA) ENSP00000512361.1:p.Asn325His
ENST00000696059.1:c.*921A>C (ADA) ENSP00000512362.1:n.*921A>C
ENST00000696060.1:c.1045A>C (ADA) ENSP00000512363.1:p.Asn349His
ENST00000696061.1:c.973A>C (ADA) ENSP00000512364.1:p.Asn325His
ENST00000696062.1:c.1039A>C (ADA) ENSP00000512365.1:p.Asn347His
ENST00000696063.1:c.1051A>C (ADA) ENSP00000512366.1:p.Asn351His
ENST00000696064.1:c.823A>C (ADA) ENSP00000512367.1:p.Asn275His
ENST00000696065.1:c.298A>C (ADA) ENSP00000512368.1:p.Asn100His
ENST00000696072.1:n.331A>C (ADA)
ENST00000696073.1:n.1287A>C (ADA)
ENST00000696074.1:n.527A>C (ADA)
ENST00000696075.1:c.*946A>C (ADA) ENSP00000512374.1:n.*946A>C
ENST00000696076.1:c.1045A>C (ADA) ENSP00000512375.1:p.Asn349His
ENST00000696077.1:c.970A>C (ADA) ENSP00000512376.1:p.Asn324His
ENST00000696078.1:c.973A>C (ADA) ENSP00000512377.1:p.Asn325His
ENST00000696079.1:c.973A>C (ADA) ENSP00000512378.1:p.Asn325His
ENST00000696080.1:c.976A>C (ADA) ENSP00000512379.1:p.Asn326His
ENST00000696081.1:n.1095A>C (ADA)
ENST00000696082.1:c.1051A>C (ADA) ENSP00000512380.1:p.Asn351His
ENST00000696083.1:n.1933A>C (ADA)
ENST00000696084.1:n.1153A>C (ADA)
ENST00000696104.1:c.*45A>C (ADA) ENSP00000512399.1:n.*45A>C
ENST00000372874.9:c.976A>C (ADA) MANE Select ENSP00000361965.4:p.Asn326His
ENST00000372874.8:c.976A>C (ADA) ENSP00000361965.4:p.Asn326His
ENST00000372887.5:c.152-3532T>G (PKIG) ENSP00000361978.1:n.152-3532T>G
ENST00000464097.5:n.1342A>C (ADA)
ENST00000492931.5:n.1136A>C (ADA)
ENST00000536532.5:c.*119A>C (ADA) ENSP00000440946.1:n.*119A>C
ENST00000537820.1:c.904A>C (ADA) ENSP00000441818.1:p.Asn302His
ENST00000539235.5:c.*360A>C (ADA) ENSP00000446464.1:n.*360A>C
NM_000022.2:c.976A>C , LRG_16t1:c.976A>C (ADA) NP_000013.2:p.Asn326His
XM_005260236.2:c.904A>C (ADA) XP_005260293.1:p.Asn302His
XM_011528478.1:c.571A>C (ADA) XP_011526780.1:p.Asn191His
XM_011528479.1:c.571A>C (ADA) XP_011526781.1:p.Asn191His
XR_244129.1:n.965A>C (ADA)
NM_000022.3:c.976A>C (ADA) NP_000013.2:p.Asn326His
NM_001322050.1:c.571A>C (ADA) NP_001308979.1:p.Asn191His
NM_001322051.1:c.904A>C (ADA) NP_001308980.1:p.Asn302His
NR_136160.1:n.1062A>C (ADA)
NM_000022.4:c.976A>C (ADA) MANE Select NP_000013.2:p.Asn326His
NM_001322050.2:c.571A>C (ADA) NP_001308979.1:p.Asn191His
NM_001322051.2:c.904A>C (ADA) NP_001308980.1:p.Asn302His
NR_136160.2:n.1003A>C (ADA)