Canonical Allele Identifier: CA1017791586

Linked Data

dbSNP Id: rs2065359920

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624180C>T , CM000682.2:g.44624180C>T GRCh38
NC_000020.10:g.43252821C>T , CM000682.1:g.43252821C>T GRCh37
NC_000020.9:g.42686235C>T NCBI36
NG_007385.1:g.32556G>A , LRG_16:g.32556G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.697+22G>A (ADA)
ENST00000536076.2:c.453+22G>A (ADA) ENSP00000512234.1:n.453+22G>A
ENST00000536532.6:c.606+22G>A (ADA) ENSP00000440946.1:n.606+22G>A
ENST00000537820.2:c.606+22G>A (ADA) ENSP00000441818.1:n.606+22G>A
ENST00000539235.6:c.219-1102G>A (ADA) ENSP00000446464.1:n.219-1102G>A
ENST00000695889.1:c.219-1250G>A (ADA) ENSP00000512240.1:n.219-1250G>A
ENST00000695890.1:n.2409+22G>A (ADA)
ENST00000695891.1:c.219-1250G>A (ADA) ENSP00000512241.1:n.219-1250G>A
ENST00000695927.1:c.684+22G>A (ADA) ENSP00000512270.1:n.684+22G>A
ENST00000695949.1:c.603+22G>A (ADA) ENSP00000512281.1:n.603+22G>A
ENST00000695957.1:c.*97+22G>A (ADA) ENSP00000512286.1:n.*97+22G>A
ENST00000695991.1:c.217-1250G>A (ADA) ENSP00000512314.1:n.217-1250G>A
ENST00000695992.1:c.606+22G>A (ADA) ENSP00000512315.1:n.606+22G>A
ENST00000695993.1:c.606+22G>A (ADA) ENSP00000512316.1:n.606+22G>A
ENST00000695994.1:c.606+22G>A (ADA) ENSP00000512317.1:n.606+22G>A
ENST00000695995.1:c.217-1102G>A (ADA) ENSP00000512318.1:n.217-1102G>A
ENST00000695996.1:n.677+22G>A (ADA)
ENST00000695997.1:n.583G>A (ADA)
ENST00000696003.1:n.698+22G>A (ADA)
ENST00000696004.1:n.698+22G>A (ADA)
ENST00000696005.1:c.128+22G>A (ADA)
ENST00000696006.1:c.606+22G>A (ADA) ENSP00000512325.1:n.606+22G>A
ENST00000696007.1:c.457+22G>A (ADA) ENSP00000512326.1:n.457+22G>A
ENST00000696008.1:n.1783G>A (ADA)
ENST00000696009.1:n.1978G>A (ADA)
ENST00000696017.1:c.603+22G>A (ADA) ENSP00000512333.1:n.603+22G>A
ENST00000696034.1:c.606+22G>A (ADA) ENSP00000512343.1:n.606+22G>A
ENST00000696035.1:n.716+22G>A (ADA)
ENST00000696036.1:n.1296+22G>A (ADA)
ENST00000696037.1:n.2283+22G>A (ADA)
ENST00000696038.1:c.*352+22G>A (ADA) ENSP00000512344.1:n.*352+22G>A
ENST00000696039.1:n.894+22G>A (ADA)
ENST00000696058.1:c.606+22G>A (ADA) ENSP00000512361.1:n.606+22G>A
ENST00000696059.1:c.*551+22G>A (ADA) ENSP00000512362.1:n.*551+22G>A
ENST00000696060.1:c.606+22G>A (ADA) ENSP00000512363.1:n.606+22G>A
ENST00000696061.1:c.603+22G>A (ADA) ENSP00000512364.1:n.603+22G>A
ENST00000696062.1:c.669+22G>A (ADA) ENSP00000512365.1:n.669+22G>A
ENST00000696063.1:c.681+22G>A (ADA) ENSP00000512366.1:n.681+22G>A
ENST00000696064.1:c.453+22G>A (ADA) ENSP00000512367.1:n.453+22G>A
ENST00000696065.1:c.66-1250G>A (ADA) ENSP00000512368.1:n.66-1250G>A
ENST00000696074.1:n.222+22G>A (ADA)
ENST00000696075.1:c.*576+22G>A (ADA) ENSP00000512374.1:n.*576+22G>A
ENST00000696076.1:c.606+22G>A (ADA) ENSP00000512375.1:n.606+22G>A
ENST00000696077.1:c.603+22G>A (ADA) ENSP00000512376.1:n.603+22G>A
ENST00000696078.1:c.606+22G>A (ADA) ENSP00000512377.1:n.606+22G>A
ENST00000696079.1:c.606+22G>A (ADA) ENSP00000512378.1:n.606+22G>A
ENST00000696080.1:c.606+22G>A (ADA) ENSP00000512379.1:n.606+22G>A
ENST00000696081.1:n.725+22G>A (ADA)
ENST00000696082.1:c.684+22G>A (ADA) ENSP00000512380.1:n.684+22G>A
ENST00000696083.1:n.1487+22G>A (ADA)
ENST00000696084.1:n.707+22G>A (ADA)
ENST00000696104.1:c.363-1250G>A (ADA) ENSP00000512399.1:n.363-1250G>A
ENST00000696105.1:c.*147+22G>A (ADA) ENSP00000512400.1:n.*147+22G>A
ENST00000372874.9:c.606+22G>A (ADA) MANE Select ENSP00000361965.4:n.606+22G>A
ENST00000372874.8:c.606+22G>A (ADA) ENSP00000361965.4:n.606+22G>A
ENST00000372887.5:c.*204C>T (PKIG) ENSP00000361978.1:n.*204C>T
ENST00000464097.5:n.280+22G>A (ADA)
ENST00000492931.5:n.690+22G>A (ADA)
ENST00000536532.5:c.606+22G>A (ADA) ENSP00000440946.1:n.606+22G>A
ENST00000537820.1:c.606+22G>A (ADA) ENSP00000441818.1:n.606+22G>A
ENST00000539235.5:c.219-1102G>A (ADA) ENSP00000446464.1:n.219-1102G>A
NM_000022.2:c.606+22G>A , LRG_16t1:c.606+22G>A (ADA) NP_000013.2:n.606+22G>A
XM_005260236.2:c.606+22G>A (ADA) XP_005260293.1:n.606+22G>A
XM_011528478.1:c.201+22G>A (ADA) XP_011526780.1:n.201+22G>A
XM_011528479.1:c.201+22G>A (ADA) XP_011526781.1:n.201+22G>A
XR_244129.1:n.660+22G>A (ADA)
NM_000022.3:c.606+22G>A (ADA) NP_000013.2:n.606+22G>A
NM_001322050.1:c.201+22G>A (ADA) NP_001308979.1:n.201+22G>A
NM_001322051.1:c.606+22G>A (ADA) NP_001308980.1:n.606+22G>A
NR_136160.1:n.757+22G>A (ADA)
NM_000022.4:c.606+22G>A (ADA) MANE Select NP_000013.2:n.606+22G>A
NM_001322050.2:c.201+22G>A (ADA) NP_001308979.1:n.201+22G>A
NM_001322051.2:c.606+22G>A (ADA) NP_001308980.1:n.606+22G>A
NR_136160.2:n.698+22G>A (ADA)