Canonical Allele Identifier: CA510593492

Linked Data

MyVariant Identifiers: chr20:g.43251657T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623016T>C , CM000682.2:g.44623016T>C GRCh38
NC_000020.10:g.43251657T>C , CM000682.1:g.43251657T>C GRCh37
NC_000020.9:g.42685071T>C NCBI36
NG_007385.1:g.33720A>G , LRG_16:g.33720A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.760A>G (ADA)
ENST00000536076.2:c.516A>G (ADA) ENSP00000512234.1:p.Val172=
ENST00000536532.6:c.669A>G (ADA) ENSP00000440946.1:p.Val223=
ENST00000537820.2:c.607-86A>G (ADA) ENSP00000441818.1:n.607-86A>G
ENST00000539235.6:c.*53A>G (ADA) ENSP00000446464.1:n.*53A>G
ENST00000695889.1:c.219-86A>G (ADA) ENSP00000512240.1:n.219-86A>G
ENST00000695890.1:n.2472A>G (ADA)
ENST00000695891.1:c.219-86A>G (ADA) ENSP00000512241.1:n.219-86A>G
ENST00000695927.1:c.747A>G (ADA) ENSP00000512270.1:p.Val249=
ENST00000695949.1:c.604-86A>G (ADA) ENSP00000512281.1:n.604-86A>G
ENST00000695957.1:c.*160A>G (ADA) ENSP00000512286.1:n.*160A>G
ENST00000695991.1:c.217-86A>G (ADA) ENSP00000512314.1:n.217-86A>G
ENST00000695992.1:c.669A>G (ADA) ENSP00000512315.1:p.Val223=
ENST00000695993.1:c.669A>G (ADA) ENSP00000512316.1:p.Val223=
ENST00000695994.1:c.651+18A>G (ADA) ENSP00000512317.1:n.651+18A>G
ENST00000695995.1:c.279A>G (ADA) ENSP00000512318.1:p.Val93=
ENST00000695996.1:n.740A>G (ADA)
ENST00000696003.1:n.761A>G (ADA)
ENST00000696004.1:n.761A>G (ADA)
ENST00000696005.1:c.129-86A>G (ADA)
ENST00000696006.1:c.607-86A>G (ADA) ENSP00000512325.1:n.607-86A>G
ENST00000696007.1:c.520A>G (ADA) ENSP00000512326.1:n.520A>G
ENST00000696008.1:n.2947A>G (ADA)
ENST00000696017.1:c.666A>G (ADA) ENSP00000512333.1:p.Val222=
ENST00000696034.1:c.669A>G (ADA) ENSP00000512343.1:p.Val223=
ENST00000696035.1:n.779A>G (ADA)
ENST00000696036.1:n.1359A>G (ADA)
ENST00000696037.1:n.2346A>G (ADA)
ENST00000696038.1:c.*415A>G (ADA) ENSP00000512344.1:n.*415A>G
ENST00000696039.1:n.957A>G (ADA)
ENST00000696058.1:c.666A>G (ADA) ENSP00000512361.1:p.Val222=
ENST00000696059.1:c.*614A>G (ADA) ENSP00000512362.1:n.*614A>G
ENST00000696060.1:c.738A>G (ADA) ENSP00000512363.1:p.Val246=
ENST00000696061.1:c.666A>G (ADA) ENSP00000512364.1:p.Val222=
ENST00000696062.1:c.732A>G (ADA) ENSP00000512365.1:p.Val244=
ENST00000696063.1:c.744A>G (ADA) ENSP00000512366.1:p.Val248=
ENST00000696064.1:c.516A>G (ADA) ENSP00000512367.1:p.Val172=
ENST00000696065.1:c.66-86A>G (ADA) ENSP00000512368.1:n.66-86A>G
ENST00000696073.1:n.904A>G (ADA)
ENST00000696074.1:n.285A>G (ADA)
ENST00000696075.1:c.*639A>G (ADA) ENSP00000512374.1:n.*639A>G
ENST00000696076.1:c.738A>G (ADA) ENSP00000512375.1:p.Val246=
ENST00000696077.1:c.663A>G (ADA) ENSP00000512376.1:p.Val221=
ENST00000696078.1:c.666A>G (ADA) ENSP00000512377.1:p.Val222=
ENST00000696079.1:c.666A>G (ADA) ENSP00000512378.1:p.Val222=
ENST00000696080.1:c.669A>G (ADA) ENSP00000512379.1:p.Val223=
ENST00000696081.1:n.788A>G (ADA)
ENST00000696082.1:c.744A>G (ADA) ENSP00000512380.1:p.Val248=
ENST00000696083.1:n.1550A>G (ADA)
ENST00000696084.1:n.770A>G (ADA)
ENST00000696104.1:c.363-86A>G (ADA) ENSP00000512399.1:n.363-86A>G
ENST00000696105.1:c.*210A>G (ADA) ENSP00000512400.1:n.*210A>G
ENST00000372874.9:c.669A>G (ADA) MANE Select ENSP00000361965.4:p.Val223=
ENST00000372874.8:c.669A>G (ADA) ENSP00000361965.4:p.Val223=
ENST00000372887.5:c.152-917T>C (PKIG) ENSP00000361978.1:n.152-917T>C
ENST00000464097.5:n.343A>G (ADA)
ENST00000492931.5:n.753A>G (ADA)
ENST00000536532.5:c.669A>G (ADA) ENSP00000440946.1:p.Val223=
ENST00000537820.1:c.607-86A>G (ADA) ENSP00000441818.1:n.607-86A>G
ENST00000539235.5:c.*53A>G (ADA) ENSP00000446464.1:n.*53A>G
NM_000022.2:c.669A>G , LRG_16t1:c.669A>G (ADA) NP_000013.2:p.Val223=
XM_005260236.2:c.607-86A>G (ADA) XP_005260293.1:n.607-86A>G
XM_011528478.1:c.264A>G (ADA) XP_011526780.1:p.Val88=
XM_011528479.1:c.264A>G (ADA) XP_011526781.1:p.Val88=
XR_244129.1:n.723A>G (ADA)
NM_000022.3:c.669A>G (ADA) NP_000013.2:p.Val223=
NM_001322050.1:c.264A>G (ADA) NP_001308979.1:p.Val88=
NM_001322051.1:c.607-86A>G (ADA) NP_001308980.1:n.607-86A>G
NR_136160.1:n.820A>G (ADA)
NM_000022.4:c.669A>G (ADA) MANE Select NP_000013.2:p.Val223=
NM_001322050.2:c.264A>G (ADA) NP_001308979.1:p.Val88=
NM_001322051.2:c.607-86A>G (ADA) NP_001308980.1:n.607-86A>G
NR_136160.2:n.761A>G (ADA)