Canonical Allele Identifier: CA9871583

Linked Data

ClinVar Variation Id: 767626
dbSNP Id: rs373256688

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623064G>A , CM000682.2:g.44623064G>A GRCh38
NC_000020.10:g.43251705G>A , CM000682.1:g.43251705G>A GRCh37
NC_000020.9:g.42685119G>A NCBI36
NG_007385.1:g.33672C>T , LRG_16:g.33672C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.712C>T (ADA)
ENST00000536076.2:c.468C>T (ADA) ENSP00000512234.1:p.Ser156=
ENST00000536532.6:c.621C>T (ADA) ENSP00000440946.1:p.Ser207=
ENST00000537820.2:c.607-134C>T (ADA) ENSP00000441818.1:n.607-134C>T
ENST00000539235.6:c.*5C>T (ADA) ENSP00000446464.1:n.*5C>T
ENST00000695889.1:c.219-134C>T (ADA) ENSP00000512240.1:n.219-134C>T
ENST00000695890.1:n.2424C>T (ADA)
ENST00000695891.1:c.219-134C>T (ADA) ENSP00000512241.1:n.219-134C>T
ENST00000695927.1:c.699C>T (ADA) ENSP00000512270.1:p.Ser233=
ENST00000695949.1:c.604-134C>T (ADA) ENSP00000512281.1:n.604-134C>T
ENST00000695957.1:c.*112C>T (ADA) ENSP00000512286.1:n.*112C>T
ENST00000695991.1:c.217-134C>T (ADA) ENSP00000512314.1:n.217-134C>T
ENST00000695992.1:c.621C>T (ADA) ENSP00000512315.1:p.Ser207=
ENST00000695993.1:c.621C>T (ADA) ENSP00000512316.1:p.Ser207=
ENST00000695994.1:c.621C>T (ADA) ENSP00000512317.1:p.Ser207=
ENST00000695995.1:c.231C>T (ADA) ENSP00000512318.1:p.Ser77=
ENST00000695996.1:n.692C>T (ADA)
ENST00000696003.1:n.713C>T (ADA)
ENST00000696004.1:n.713C>T (ADA)
ENST00000696005.1:c.129-134C>T (ADA)
ENST00000696006.1:c.607-134C>T (ADA) ENSP00000512325.1:n.607-134C>T
ENST00000696007.1:c.472C>T (ADA) ENSP00000512326.1:n.472C>T
ENST00000696008.1:n.2899C>T (ADA)
ENST00000696017.1:c.618C>T (ADA) ENSP00000512333.1:p.Ser206=
ENST00000696034.1:c.621C>T (ADA) ENSP00000512343.1:p.Ser207=
ENST00000696035.1:n.731C>T (ADA)
ENST00000696036.1:n.1311C>T (ADA)
ENST00000696037.1:n.2298C>T (ADA)
ENST00000696038.1:c.*367C>T (ADA) ENSP00000512344.1:n.*367C>T
ENST00000696039.1:n.909C>T (ADA)
ENST00000696058.1:c.618C>T (ADA) ENSP00000512361.1:p.Ser206=
ENST00000696059.1:c.*566C>T (ADA) ENSP00000512362.1:n.*566C>T
ENST00000696060.1:c.690C>T (ADA) ENSP00000512363.1:p.Ser230=
ENST00000696061.1:c.618C>T (ADA) ENSP00000512364.1:p.Ser206=
ENST00000696062.1:c.684C>T (ADA) ENSP00000512365.1:p.Ser228=
ENST00000696063.1:c.696C>T (ADA) ENSP00000512366.1:p.Ser232=
ENST00000696064.1:c.468C>T (ADA) ENSP00000512367.1:p.Ser156=
ENST00000696065.1:c.66-134C>T (ADA) ENSP00000512368.1:n.66-134C>T
ENST00000696073.1:n.856C>T (ADA)
ENST00000696074.1:n.237C>T (ADA)
ENST00000696075.1:c.*591C>T (ADA) ENSP00000512374.1:n.*591C>T
ENST00000696076.1:c.690C>T (ADA) ENSP00000512375.1:p.Ser230=
ENST00000696077.1:c.615C>T (ADA) ENSP00000512376.1:p.Ser205=
ENST00000696078.1:c.618C>T (ADA) ENSP00000512377.1:p.Ser206=
ENST00000696079.1:c.618C>T (ADA) ENSP00000512378.1:p.Ser206=
ENST00000696080.1:c.621C>T (ADA) ENSP00000512379.1:p.Ser207=
ENST00000696081.1:n.740C>T (ADA)
ENST00000696082.1:c.696C>T (ADA) ENSP00000512380.1:p.Ser232=
ENST00000696083.1:n.1502C>T (ADA)
ENST00000696084.1:n.722C>T (ADA)
ENST00000696104.1:c.363-134C>T (ADA) ENSP00000512399.1:n.363-134C>T
ENST00000696105.1:c.*162C>T (ADA) ENSP00000512400.1:n.*162C>T
ENST00000372874.9:c.621C>T (ADA) MANE Select ENSP00000361965.4:p.Ser207=
ENST00000372874.8:c.621C>T (ADA) ENSP00000361965.4:p.Ser207=
ENST00000372887.5:c.152-869G>A (PKIG) ENSP00000361978.1:n.152-869G>A
ENST00000464097.5:n.295C>T (ADA)
ENST00000492931.5:n.705C>T (ADA)
ENST00000536532.5:c.621C>T (ADA) ENSP00000440946.1:p.Ser207=
ENST00000537820.1:c.607-134C>T (ADA) ENSP00000441818.1:n.607-134C>T
ENST00000539235.5:c.*5C>T (ADA) ENSP00000446464.1:n.*5C>T
NM_000022.2:c.621C>T , LRG_16t1:c.621C>T (ADA) NP_000013.2:p.Ser207=
XM_005260236.2:c.607-134C>T (ADA) XP_005260293.1:n.607-134C>T
XM_011528478.1:c.216C>T (ADA) XP_011526780.1:p.Ser72=
XM_011528479.1:c.216C>T (ADA) XP_011526781.1:p.Ser72=
XR_244129.1:n.675C>T (ADA)
NM_000022.3:c.621C>T (ADA) NP_000013.2:p.Ser207=
NM_001322050.1:c.216C>T (ADA) NP_001308979.1:p.Ser72=
NM_001322051.1:c.607-134C>T (ADA) NP_001308980.1:n.607-134C>T
NR_136160.1:n.772C>T (ADA)
NM_000022.4:c.621C>T (ADA) MANE Select NP_000013.2:p.Ser207=
NM_001322050.2:c.216C>T (ADA) NP_001308979.1:p.Ser72=
NM_001322051.2:c.607-134C>T (ADA) NP_001308980.1:n.607-134C>T
NR_136160.2:n.713C>T (ADA)