Canonical Allele Identifier: CA409120491

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623065C>T , CM000682.2:g.44623065C>T GRCh38
NC_000020.10:g.43251706C>T , CM000682.1:g.43251706C>T GRCh37
NC_000020.9:g.42685120C>T NCBI36
NG_007385.1:g.33671G>A , LRG_16:g.33671G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.711G>A (ADA)
ENST00000536076.2:c.467G>A (ADA) ENSP00000512234.1:p.Ser156Asn
ENST00000536532.6:c.620G>A (ADA) ENSP00000440946.1:p.Ser207Asn
ENST00000537820.2:c.607-135G>A (ADA) ENSP00000441818.1:n.607-135G>A
ENST00000539235.6:c.*4G>A (ADA) ENSP00000446464.1:n.*4G>A
ENST00000695889.1:c.219-135G>A (ADA) ENSP00000512240.1:n.219-135G>A
ENST00000695890.1:n.2423G>A (ADA)
ENST00000695891.1:c.219-135G>A (ADA) ENSP00000512241.1:n.219-135G>A
ENST00000695927.1:c.698G>A (ADA) ENSP00000512270.1:p.Ser233Asn
ENST00000695949.1:c.604-135G>A (ADA) ENSP00000512281.1:n.604-135G>A
ENST00000695957.1:c.*111G>A (ADA) ENSP00000512286.1:n.*111G>A
ENST00000695991.1:c.217-135G>A (ADA) ENSP00000512314.1:n.217-135G>A
ENST00000695992.1:c.620G>A (ADA) ENSP00000512315.1:p.Ser207Asn
ENST00000695993.1:c.620G>A (ADA) ENSP00000512316.1:p.Ser207Asn
ENST00000695994.1:c.620G>A (ADA) ENSP00000512317.1:p.Ser207Asn
ENST00000695995.1:c.230G>A (ADA) ENSP00000512318.1:p.Ser77Asn
ENST00000695996.1:n.691G>A (ADA)
ENST00000696003.1:n.712G>A (ADA)
ENST00000696004.1:n.712G>A (ADA)
ENST00000696005.1:c.129-135G>A (ADA)
ENST00000696006.1:c.607-135G>A (ADA) ENSP00000512325.1:n.607-135G>A
ENST00000696007.1:c.471G>A (ADA) ENSP00000512326.1:n.471G>A
ENST00000696008.1:n.2898G>A (ADA)
ENST00000696017.1:c.617G>A (ADA) ENSP00000512333.1:p.Ser206Asn
ENST00000696034.1:c.620G>A (ADA) ENSP00000512343.1:p.Ser207Asn
ENST00000696035.1:n.730G>A (ADA)
ENST00000696036.1:n.1310G>A (ADA)
ENST00000696037.1:n.2297G>A (ADA)
ENST00000696038.1:c.*366G>A (ADA) ENSP00000512344.1:n.*366G>A
ENST00000696039.1:n.908G>A (ADA)
ENST00000696058.1:c.617G>A (ADA) ENSP00000512361.1:p.Ser206Asn
ENST00000696059.1:c.*565G>A (ADA) ENSP00000512362.1:n.*565G>A
ENST00000696060.1:c.689G>A (ADA) ENSP00000512363.1:p.Ser230Asn
ENST00000696061.1:c.617G>A (ADA) ENSP00000512364.1:p.Ser206Asn
ENST00000696062.1:c.683G>A (ADA) ENSP00000512365.1:p.Ser228Asn
ENST00000696063.1:c.695G>A (ADA) ENSP00000512366.1:p.Ser232Asn
ENST00000696064.1:c.467G>A (ADA) ENSP00000512367.1:p.Ser156Asn
ENST00000696065.1:c.66-135G>A (ADA) ENSP00000512368.1:n.66-135G>A
ENST00000696073.1:n.855G>A (ADA)
ENST00000696074.1:n.236G>A (ADA)
ENST00000696075.1:c.*590G>A (ADA) ENSP00000512374.1:n.*590G>A
ENST00000696076.1:c.689G>A (ADA) ENSP00000512375.1:p.Ser230Asn
ENST00000696077.1:c.614G>A (ADA) ENSP00000512376.1:p.Ser205Asn
ENST00000696078.1:c.617G>A (ADA) ENSP00000512377.1:p.Ser206Asn
ENST00000696079.1:c.617G>A (ADA) ENSP00000512378.1:p.Ser206Asn
ENST00000696080.1:c.620G>A (ADA) ENSP00000512379.1:p.Ser207Asn
ENST00000696081.1:n.739G>A (ADA)
ENST00000696082.1:c.695G>A (ADA) ENSP00000512380.1:p.Ser232Asn
ENST00000696083.1:n.1501G>A (ADA)
ENST00000696084.1:n.721G>A (ADA)
ENST00000696104.1:c.363-135G>A (ADA) ENSP00000512399.1:n.363-135G>A
ENST00000696105.1:c.*161G>A (ADA) ENSP00000512400.1:n.*161G>A
ENST00000372874.9:c.620G>A (ADA) MANE Select ENSP00000361965.4:p.Ser207Asn
ENST00000372874.8:c.620G>A (ADA) ENSP00000361965.4:p.Ser207Asn
ENST00000372887.5:c.152-868C>T (PKIG) ENSP00000361978.1:n.152-868C>T
ENST00000464097.5:n.294G>A (ADA)
ENST00000492931.5:n.704G>A (ADA)
ENST00000536532.5:c.620G>A (ADA) ENSP00000440946.1:p.Ser207Asn
ENST00000537820.1:c.607-135G>A (ADA) ENSP00000441818.1:n.607-135G>A
ENST00000539235.5:c.*4G>A (ADA) ENSP00000446464.1:n.*4G>A
NM_000022.2:c.620G>A , LRG_16t1:c.620G>A (ADA) NP_000013.2:p.Ser207Asn
XM_005260236.2:c.607-135G>A (ADA) XP_005260293.1:n.607-135G>A
XM_011528478.1:c.215G>A (ADA) XP_011526780.1:p.Ser72Asn
XM_011528479.1:c.215G>A (ADA) XP_011526781.1:p.Ser72Asn
XR_244129.1:n.674G>A (ADA)
NM_000022.3:c.620G>A (ADA) NP_000013.2:p.Ser207Asn
NM_001322050.1:c.215G>A (ADA) NP_001308979.1:p.Ser72Asn
NM_001322051.1:c.607-135G>A (ADA) NP_001308980.1:n.607-135G>A
NR_136160.1:n.771G>A (ADA)
NM_000022.4:c.620G>A (ADA) MANE Select NP_000013.2:p.Ser207Asn
NM_001322050.2:c.215G>A (ADA) NP_001308979.1:p.Ser72Asn
NM_001322051.2:c.607-135G>A (ADA) NP_001308980.1:n.607-135G>A
NR_136160.2:n.712G>A (ADA)