Canonical Allele Identifier: CA266022

Linked Data

ClinVar Variation Id: 68268
ClinVar RCV Id: RCV000059110
dbSNP Id: rs121908734

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44624212T>G , CM000682.2:g.44624212T>G GRCh38
NC_000020.10:g.43252853T>G , CM000682.1:g.43252853T>G GRCh37
NC_000020.9:g.42686267T>G NCBI36
NG_007385.1:g.32524A>C , LRG_16:g.32524A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.687A>C (ADA)
ENST00000536076.2:c.443A>C (ADA) ENSP00000512234.1:p.Gln148Pro
ENST00000536532.6:c.596A>C (ADA) ENSP00000440946.1:p.Gln199Pro
ENST00000537820.2:c.596A>C (ADA) ENSP00000441818.1:p.Gln199Pro
ENST00000539235.6:c.219-1134A>C (ADA) ENSP00000446464.1:n.219-1134A>C
ENST00000695889.1:c.219-1282A>C (ADA) ENSP00000512240.1:n.219-1282A>C
ENST00000695890.1:n.2399A>C (ADA)
ENST00000695891.1:c.219-1282A>C (ADA) ENSP00000512241.1:n.219-1282A>C
ENST00000695927.1:c.674A>C (ADA) ENSP00000512270.1:p.Gln225Pro
ENST00000695949.1:c.593A>C (ADA) ENSP00000512281.1:p.Gln198Pro
ENST00000695957.1:c.*87A>C (ADA) ENSP00000512286.1:n.*87A>C
ENST00000695991.1:c.217-1282A>C (ADA) ENSP00000512314.1:n.217-1282A>C
ENST00000695992.1:c.596A>C (ADA) ENSP00000512315.1:p.Gln199Pro
ENST00000695993.1:c.596A>C (ADA) ENSP00000512316.1:p.Gln199Pro
ENST00000695994.1:c.596A>C (ADA) ENSP00000512317.1:p.Gln199Pro
ENST00000695995.1:c.217-1134A>C (ADA) ENSP00000512318.1:n.217-1134A>C
ENST00000695996.1:n.667A>C (ADA)
ENST00000695997.1:n.551A>C (ADA)
ENST00000696003.1:n.688A>C (ADA)
ENST00000696004.1:n.688A>C (ADA)
ENST00000696005.1:c.118A>C (ADA)
ENST00000696006.1:c.596A>C (ADA) ENSP00000512325.1:p.Gln199Pro
ENST00000696007.1:c.447A>C (ADA) ENSP00000512326.1:n.447A>C
ENST00000696008.1:n.1751A>C (ADA)
ENST00000696009.1:n.1946A>C (ADA)
ENST00000696017.1:c.593A>C (ADA) ENSP00000512333.1:p.Gln198Pro
ENST00000696034.1:c.596A>C (ADA) ENSP00000512343.1:p.Gln199Pro
ENST00000696035.1:n.706A>C (ADA)
ENST00000696036.1:n.1286A>C (ADA)
ENST00000696037.1:n.2273A>C (ADA)
ENST00000696038.1:c.*342A>C (ADA) ENSP00000512344.1:n.*342A>C
ENST00000696039.1:n.884A>C (ADA)
ENST00000696058.1:c.596A>C (ADA) ENSP00000512361.1:p.Gln199Pro
ENST00000696059.1:c.*541A>C (ADA) ENSP00000512362.1:n.*541A>C
ENST00000696060.1:c.596A>C (ADA) ENSP00000512363.1:p.Gln199Pro
ENST00000696061.1:c.593A>C (ADA) ENSP00000512364.1:p.Gln198Pro
ENST00000696062.1:c.659A>C (ADA) ENSP00000512365.1:p.Gln220Pro
ENST00000696063.1:c.671A>C (ADA) ENSP00000512366.1:p.Gln224Pro
ENST00000696064.1:c.443A>C (ADA) ENSP00000512367.1:p.Gln148Pro
ENST00000696065.1:c.66-1282A>C (ADA) ENSP00000512368.1:n.66-1282A>C
ENST00000696074.1:n.212A>C (ADA)
ENST00000696075.1:c.*566A>C (ADA) ENSP00000512374.1:n.*566A>C
ENST00000696076.1:c.596A>C (ADA) ENSP00000512375.1:p.Gln199Pro
ENST00000696077.1:c.593A>C (ADA) ENSP00000512376.1:p.Gln198Pro
ENST00000696078.1:c.596A>C (ADA) ENSP00000512377.1:p.Gln199Pro
ENST00000696079.1:c.596A>C (ADA) ENSP00000512378.1:p.Gln199Pro
ENST00000696080.1:c.596A>C (ADA) ENSP00000512379.1:p.Gln199Pro
ENST00000696081.1:n.715A>C (ADA)
ENST00000696082.1:c.674A>C (ADA) ENSP00000512380.1:p.Gln225Pro
ENST00000696083.1:n.1477A>C (ADA)
ENST00000696084.1:n.697A>C (ADA)
ENST00000696104.1:c.363-1282A>C (ADA) ENSP00000512399.1:n.363-1282A>C
ENST00000696105.1:c.*137A>C (ADA) ENSP00000512400.1:n.*137A>C
ENST00000372874.9:c.596A>C (ADA) MANE Select ENSP00000361965.4:p.Gln199Pro
ENST00000372874.8:c.596A>C (ADA) ENSP00000361965.4:p.Gln199Pro
ENST00000372887.5:c.*236T>G (PKIG) ENSP00000361978.1:n.*236T>G
ENST00000464097.5:n.270A>C (ADA)
ENST00000492931.5:n.680A>C (ADA)
ENST00000536532.5:c.596A>C (ADA) ENSP00000440946.1:p.Gln199Pro
ENST00000537820.1:c.596A>C (ADA) ENSP00000441818.1:p.Gln199Pro
ENST00000539235.5:c.219-1134A>C (ADA) ENSP00000446464.1:n.219-1134A>C
NM_000022.2:c.596A>C , LRG_16t1:c.596A>C (ADA) NP_000013.2:p.Gln199Pro
XM_005260236.2:c.596A>C (ADA) XP_005260293.1:p.Gln199Pro
XM_011528478.1:c.191A>C (ADA) XP_011526780.1:p.Gln64Pro
XM_011528479.1:c.191A>C (ADA) XP_011526781.1:p.Gln64Pro
XR_244129.1:n.650A>C (ADA)
NM_000022.3:c.596A>C (ADA) NP_000013.2:p.Gln199Pro
NM_001322050.1:c.191A>C (ADA) NP_001308979.1:p.Gln64Pro
NM_001322051.1:c.596A>C (ADA) NP_001308980.1:p.Gln199Pro
NR_136160.1:n.747A>C (ADA)
NM_000022.4:c.596A>C (ADA) MANE Select NP_000013.2:p.Gln199Pro
NM_001322050.2:c.191A>C (ADA) NP_001308979.1:p.Gln64Pro
NM_001322051.2:c.596A>C (ADA) NP_001308980.1:p.Gln199Pro
NR_136160.2:n.688A>C (ADA)