Canonical Allele Identifier: CA1017791242

Linked Data

dbSNP Id: rs2065350287

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623224C>A , CM000682.2:g.44623224C>A GRCh38
NC_000020.10:g.43251865C>A , CM000682.1:g.43251865C>A GRCh37
NC_000020.9:g.42685279C>A NCBI36
NG_007385.1:g.33512G>T , LRG_16:g.33512G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.698-146G>T (ADA)
ENST00000536076.2:c.454-146G>T (ADA) ENSP00000512234.1:n.454-146G>T
ENST00000536532.6:c.607-146G>T (ADA) ENSP00000440946.1:n.607-146G>T
ENST00000537820.2:c.607-294G>T (ADA) ENSP00000441818.1:n.607-294G>T
ENST00000539235.6:c.219-146G>T (ADA) ENSP00000446464.1:n.219-146G>T
ENST00000695889.1:c.219-294G>T (ADA) ENSP00000512240.1:n.219-294G>T
ENST00000695890.1:n.2410-146G>T (ADA)
ENST00000695891.1:c.219-294G>T (ADA) ENSP00000512241.1:n.219-294G>T
ENST00000695927.1:c.685-146G>T (ADA) ENSP00000512270.1:n.685-146G>T
ENST00000695949.1:c.604-294G>T (ADA) ENSP00000512281.1:n.604-294G>T
ENST00000695957.1:c.*98-146G>T (ADA) ENSP00000512286.1:n.*98-146G>T
ENST00000695991.1:c.217-294G>T (ADA) ENSP00000512314.1:n.217-294G>T
ENST00000695992.1:c.607-146G>T (ADA) ENSP00000512315.1:n.607-146G>T
ENST00000695993.1:c.607-146G>T (ADA) ENSP00000512316.1:n.607-146G>T
ENST00000695994.1:c.607-146G>T (ADA) ENSP00000512317.1:n.607-146G>T
ENST00000695995.1:c.217-146G>T (ADA) ENSP00000512318.1:n.217-146G>T
ENST00000695996.1:n.678-146G>T (ADA)
ENST00000696003.1:n.699-146G>T (ADA)
ENST00000696004.1:n.699-146G>T (ADA)
ENST00000696005.1:c.129-294G>T (ADA)
ENST00000696006.1:c.607-294G>T (ADA) ENSP00000512325.1:n.607-294G>T
ENST00000696007.1:c.458-146G>T (ADA) ENSP00000512326.1:n.458-146G>T
ENST00000696008.1:n.2739G>T (ADA)
ENST00000696017.1:c.604-146G>T (ADA) ENSP00000512333.1:n.604-146G>T
ENST00000696034.1:c.607-146G>T (ADA) ENSP00000512343.1:n.607-146G>T
ENST00000696035.1:n.717-146G>T (ADA)
ENST00000696036.1:n.1297-146G>T (ADA)
ENST00000696037.1:n.2284-146G>T (ADA)
ENST00000696038.1:c.*353-146G>T (ADA) ENSP00000512344.1:n.*353-146G>T
ENST00000696039.1:n.895-146G>T (ADA)
ENST00000696058.1:c.607-149G>T (ADA) ENSP00000512361.1:n.607-149G>T
ENST00000696059.1:c.*552-146G>T (ADA) ENSP00000512362.1:n.*552-146G>T
ENST00000696060.1:c.607-77G>T (ADA) ENSP00000512363.1:n.607-77G>T
ENST00000696061.1:c.604-146G>T (ADA) ENSP00000512364.1:n.604-146G>T
ENST00000696062.1:c.670-146G>T (ADA) ENSP00000512365.1:n.670-146G>T
ENST00000696063.1:c.682-146G>T (ADA) ENSP00000512366.1:n.682-146G>T
ENST00000696064.1:c.454-146G>T (ADA) ENSP00000512367.1:n.454-146G>T
ENST00000696065.1:c.66-294G>T (ADA) ENSP00000512368.1:n.66-294G>T
ENST00000696073.1:n.696G>T (ADA)
ENST00000696074.1:n.223-146G>T (ADA)
ENST00000696075.1:c.*577-146G>T (ADA) ENSP00000512374.1:n.*577-146G>T
ENST00000696076.1:c.607-77G>T (ADA) ENSP00000512375.1:n.607-77G>T
ENST00000696077.1:c.604-149G>T (ADA) ENSP00000512376.1:n.604-149G>T
ENST00000696078.1:c.607-149G>T (ADA) ENSP00000512377.1:n.607-149G>T
ENST00000696079.1:c.607-149G>T (ADA) ENSP00000512378.1:n.607-149G>T
ENST00000696080.1:c.607-146G>T (ADA) ENSP00000512379.1:n.607-146G>T
ENST00000696081.1:n.726-146G>T (ADA)
ENST00000696082.1:c.685-149G>T (ADA) ENSP00000512380.1:n.685-149G>T
ENST00000696083.1:n.1488-146G>T (ADA)
ENST00000696084.1:n.708-146G>T (ADA)
ENST00000696104.1:c.363-294G>T (ADA) ENSP00000512399.1:n.363-294G>T
ENST00000696105.1:c.*148-146G>T (ADA) ENSP00000512400.1:n.*148-146G>T
ENST00000372874.9:c.607-146G>T (ADA) MANE Select ENSP00000361965.4:n.607-146G>T
ENST00000372874.8:c.607-146G>T (ADA) ENSP00000361965.4:n.607-146G>T
ENST00000372887.5:c.152-709C>A (PKIG) ENSP00000361978.1:n.152-709C>A
ENST00000464097.5:n.281-146G>T (ADA)
ENST00000492931.5:n.691-146G>T (ADA)
ENST00000536532.5:c.607-146G>T (ADA) ENSP00000440946.1:n.607-146G>T
ENST00000537820.1:c.607-294G>T (ADA) ENSP00000441818.1:n.607-294G>T
ENST00000539235.5:c.219-146G>T (ADA) ENSP00000446464.1:n.219-146G>T
NM_000022.2:c.607-146G>T , LRG_16t1:c.607-146G>T (ADA) NP_000013.2:n.607-146G>T
XM_005260236.2:c.607-294G>T (ADA) XP_005260293.1:n.607-294G>T
XM_011528478.1:c.202-146G>T (ADA) XP_011526780.1:n.202-146G>T
XM_011528479.1:c.202-146G>T (ADA) XP_011526781.1:n.202-146G>T
XR_244129.1:n.661-146G>T (ADA)
NM_000022.3:c.607-146G>T (ADA) NP_000013.2:n.607-146G>T
NM_001322050.1:c.202-146G>T (ADA) NP_001308979.1:n.202-146G>T
NM_001322051.1:c.607-294G>T (ADA) NP_001308980.1:n.607-294G>T
NR_136160.1:n.758-146G>T (ADA)
NM_000022.4:c.607-146G>T (ADA) MANE Select NP_000013.2:n.607-146G>T
NM_001322050.2:c.202-146G>T (ADA) NP_001308979.1:n.202-146G>T
NM_001322051.2:c.607-294G>T (ADA) NP_001308980.1:n.607-294G>T
NR_136160.2:n.699-146G>T (ADA)