Canonical Allele Identifier: CA409120406

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623023G>A , CM000682.2:g.44623023G>A GRCh38
NC_000020.10:g.43251664G>A , CM000682.1:g.43251664G>A GRCh37
NC_000020.9:g.42685078G>A NCBI36
NG_007385.1:g.33713C>T , LRG_16:g.33713C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.753C>T (ADA)
ENST00000536076.2:c.509C>T (ADA) ENSP00000512234.1:p.Ala170Val
ENST00000536532.6:c.662C>T (ADA) ENSP00000440946.1:p.Ala221Val
ENST00000537820.2:c.607-93C>T (ADA) ENSP00000441818.1:n.607-93C>T
ENST00000539235.6:c.*46C>T (ADA) ENSP00000446464.1:n.*46C>T
ENST00000695889.1:c.219-93C>T (ADA) ENSP00000512240.1:n.219-93C>T
ENST00000695890.1:n.2465C>T (ADA)
ENST00000695891.1:c.219-93C>T (ADA) ENSP00000512241.1:n.219-93C>T
ENST00000695927.1:c.740C>T (ADA) ENSP00000512270.1:p.Ala247Val
ENST00000695949.1:c.604-93C>T (ADA) ENSP00000512281.1:n.604-93C>T
ENST00000695957.1:c.*153C>T (ADA) ENSP00000512286.1:n.*153C>T
ENST00000695991.1:c.217-93C>T (ADA) ENSP00000512314.1:n.217-93C>T
ENST00000695992.1:c.662C>T (ADA) ENSP00000512315.1:p.Ala221Val
ENST00000695993.1:c.662C>T (ADA) ENSP00000512316.1:p.Ala221Val
ENST00000695994.1:c.651+11C>T (ADA) ENSP00000512317.1:n.651+11C>T
ENST00000695995.1:c.272C>T (ADA) ENSP00000512318.1:p.Ala91Val
ENST00000695996.1:n.733C>T (ADA)
ENST00000696003.1:n.754C>T (ADA)
ENST00000696004.1:n.754C>T (ADA)
ENST00000696005.1:c.129-93C>T (ADA)
ENST00000696006.1:c.607-93C>T (ADA) ENSP00000512325.1:n.607-93C>T
ENST00000696007.1:c.513C>T (ADA) ENSP00000512326.1:n.513C>T
ENST00000696008.1:n.2940C>T (ADA)
ENST00000696017.1:c.659C>T (ADA) ENSP00000512333.1:p.Ala220Val
ENST00000696034.1:c.662C>T (ADA) ENSP00000512343.1:p.Ala221Val
ENST00000696035.1:n.772C>T (ADA)
ENST00000696036.1:n.1352C>T (ADA)
ENST00000696037.1:n.2339C>T (ADA)
ENST00000696038.1:c.*408C>T (ADA) ENSP00000512344.1:n.*408C>T
ENST00000696039.1:n.950C>T (ADA)
ENST00000696058.1:c.659C>T (ADA) ENSP00000512361.1:p.Ala220Val
ENST00000696059.1:c.*607C>T (ADA) ENSP00000512362.1:n.*607C>T
ENST00000696060.1:c.731C>T (ADA) ENSP00000512363.1:p.Ala244Val
ENST00000696061.1:c.659C>T (ADA) ENSP00000512364.1:p.Ala220Val
ENST00000696062.1:c.725C>T (ADA) ENSP00000512365.1:p.Ala242Val
ENST00000696063.1:c.737C>T (ADA) ENSP00000512366.1:p.Ala246Val
ENST00000696064.1:c.509C>T (ADA) ENSP00000512367.1:p.Ala170Val
ENST00000696065.1:c.66-93C>T (ADA) ENSP00000512368.1:n.66-93C>T
ENST00000696073.1:n.897C>T (ADA)
ENST00000696074.1:n.278C>T (ADA)
ENST00000696075.1:c.*632C>T (ADA) ENSP00000512374.1:n.*632C>T
ENST00000696076.1:c.731C>T (ADA) ENSP00000512375.1:p.Ala244Val
ENST00000696077.1:c.656C>T (ADA) ENSP00000512376.1:p.Ala219Val
ENST00000696078.1:c.659C>T (ADA) ENSP00000512377.1:p.Ala220Val
ENST00000696079.1:c.659C>T (ADA) ENSP00000512378.1:p.Ala220Val
ENST00000696080.1:c.662C>T (ADA) ENSP00000512379.1:p.Ala221Val
ENST00000696081.1:n.781C>T (ADA)
ENST00000696082.1:c.737C>T (ADA) ENSP00000512380.1:p.Ala246Val
ENST00000696083.1:n.1543C>T (ADA)
ENST00000696084.1:n.763C>T (ADA)
ENST00000696104.1:c.363-93C>T (ADA) ENSP00000512399.1:n.363-93C>T
ENST00000696105.1:c.*203C>T (ADA) ENSP00000512400.1:n.*203C>T
ENST00000372874.9:c.662C>T (ADA) MANE Select ENSP00000361965.4:p.Ala221Val
ENST00000372874.8:c.662C>T (ADA) ENSP00000361965.4:p.Ala221Val
ENST00000372887.5:c.152-910G>A (PKIG) ENSP00000361978.1:n.152-910G>A
ENST00000464097.5:n.336C>T (ADA)
ENST00000492931.5:n.746C>T (ADA)
ENST00000536532.5:c.662C>T (ADA) ENSP00000440946.1:p.Ala221Val
ENST00000537820.1:c.607-93C>T (ADA) ENSP00000441818.1:n.607-93C>T
ENST00000539235.5:c.*46C>T (ADA) ENSP00000446464.1:n.*46C>T
NM_000022.2:c.662C>T , LRG_16t1:c.662C>T (ADA) NP_000013.2:p.Ala221Val
XM_005260236.2:c.607-93C>T (ADA) XP_005260293.1:n.607-93C>T
XM_011528478.1:c.257C>T (ADA) XP_011526780.1:p.Ala86Val
XM_011528479.1:c.257C>T (ADA) XP_011526781.1:p.Ala86Val
XR_244129.1:n.716C>T (ADA)
NM_000022.3:c.662C>T (ADA) NP_000013.2:p.Ala221Val
NM_001322050.1:c.257C>T (ADA) NP_001308979.1:p.Ala86Val
NM_001322051.1:c.607-93C>T (ADA) NP_001308980.1:n.607-93C>T
NR_136160.1:n.813C>T (ADA)
NM_000022.4:c.662C>T (ADA) MANE Select NP_000013.2:p.Ala221Val
NM_001322050.2:c.257C>T (ADA) NP_001308979.1:p.Ala86Val
NM_001322051.2:c.607-93C>T (ADA) NP_001308980.1:n.607-93C>T
NR_136160.2:n.754C>T (ADA)