Canonical Allele Identifier: CA409120758

Gene: ADA PKIG

Linked Data

• MyVariant Identifiers: chr20:g.43252854G>C (hg19) ; chr20:g.44624213G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44624213G>C , CM000682.2:g.44624213G>C	GRCh38
NC_000020.10:g.43252854G>C , CM000682.1:g.43252854G>C	GRCh37
NC_000020.9:g.42686268G>C	NCBI36
NG_007385.1:g.32523C>G , LRG_16:g.32523C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.686C>G (ADA)
ENST00000536076.2:c.442C>G (ADA)	ENSP00000512234.1:p.Gln148Glu
ENST00000536532.6:c.595C>G (ADA)	ENSP00000440946.1:p.Gln199Glu
ENST00000537820.2:c.595C>G (ADA)	ENSP00000441818.1:p.Gln199Glu
ENST00000539235.6:c.219-1135C>G (ADA)	ENSP00000446464.1:n.219-1135C>G
ENST00000695889.1:c.219-1283C>G (ADA)	ENSP00000512240.1:n.219-1283C>G
ENST00000695890.1:n.2398C>G (ADA)
ENST00000695891.1:c.219-1283C>G (ADA)	ENSP00000512241.1:n.219-1283C>G
ENST00000695927.1:c.673C>G (ADA)	ENSP00000512270.1:p.Gln225Glu
ENST00000695949.1:c.592C>G (ADA)	ENSP00000512281.1:p.Gln198Glu
ENST00000695957.1:c.*86C>G (ADA)	ENSP00000512286.1:n.*86C>G
ENST00000695991.1:c.217-1283C>G (ADA)	ENSP00000512314.1:n.217-1283C>G
ENST00000695992.1:c.595C>G (ADA)	ENSP00000512315.1:p.Gln199Glu
ENST00000695993.1:c.595C>G (ADA)	ENSP00000512316.1:p.Gln199Glu
ENST00000695994.1:c.595C>G (ADA)	ENSP00000512317.1:p.Gln199Glu
ENST00000695995.1:c.217-1135C>G (ADA)	ENSP00000512318.1:n.217-1135C>G
ENST00000695996.1:n.666C>G (ADA)
ENST00000695997.1:n.550C>G (ADA)
ENST00000696003.1:n.687C>G (ADA)
ENST00000696004.1:n.687C>G (ADA)
ENST00000696005.1:c.117C>G (ADA)
ENST00000696006.1:c.595C>G (ADA)	ENSP00000512325.1:p.Gln199Glu
ENST00000696007.1:c.446C>G (ADA)	ENSP00000512326.1:n.446C>G
ENST00000696008.1:n.1750C>G (ADA)
ENST00000696009.1:n.1945C>G (ADA)
ENST00000696017.1:c.592C>G (ADA)	ENSP00000512333.1:p.Gln198Glu
ENST00000696034.1:c.595C>G (ADA)	ENSP00000512343.1:p.Gln199Glu
ENST00000696035.1:n.705C>G (ADA)
ENST00000696036.1:n.1285C>G (ADA)
ENST00000696037.1:n.2272C>G (ADA)
ENST00000696038.1:c.*341C>G (ADA)	ENSP00000512344.1:n.*341C>G
ENST00000696039.1:n.883C>G (ADA)
ENST00000696058.1:c.595C>G (ADA)	ENSP00000512361.1:p.Gln199Glu
ENST00000696059.1:c.*540C>G (ADA)	ENSP00000512362.1:n.*540C>G
ENST00000696060.1:c.595C>G (ADA)	ENSP00000512363.1:p.Gln199Glu
ENST00000696061.1:c.592C>G (ADA)	ENSP00000512364.1:p.Gln198Glu
ENST00000696062.1:c.658C>G (ADA)	ENSP00000512365.1:p.Gln220Glu
ENST00000696063.1:c.670C>G (ADA)	ENSP00000512366.1:p.Gln224Glu
ENST00000696064.1:c.442C>G (ADA)	ENSP00000512367.1:p.Gln148Glu
ENST00000696065.1:c.66-1283C>G (ADA)	ENSP00000512368.1:n.66-1283C>G
ENST00000696074.1:n.211C>G (ADA)
ENST00000696075.1:c.*565C>G (ADA)	ENSP00000512374.1:n.*565C>G
ENST00000696076.1:c.595C>G (ADA)	ENSP00000512375.1:p.Gln199Glu
ENST00000696077.1:c.592C>G (ADA)	ENSP00000512376.1:p.Gln198Glu
ENST00000696078.1:c.595C>G (ADA)	ENSP00000512377.1:p.Gln199Glu
ENST00000696079.1:c.595C>G (ADA)	ENSP00000512378.1:p.Gln199Glu
ENST00000696080.1:c.595C>G (ADA)	ENSP00000512379.1:p.Gln199Glu
ENST00000696081.1:n.714C>G (ADA)
ENST00000696082.1:c.673C>G (ADA)	ENSP00000512380.1:p.Gln225Glu
ENST00000696083.1:n.1476C>G (ADA)
ENST00000696084.1:n.696C>G (ADA)
ENST00000696104.1:c.363-1283C>G (ADA)	ENSP00000512399.1:n.363-1283C>G
ENST00000696105.1:c.*136C>G (ADA)	ENSP00000512400.1:n.*136C>G
ENST00000372874.9:c.595C>G (ADA) MANE Select	ENSP00000361965.4:p.Gln199Glu
ENST00000372874.8:c.595C>G (ADA)	ENSP00000361965.4:p.Gln199Glu
ENST00000372887.5:c.*237G>C (PKIG)	ENSP00000361978.1:n.*237G>C
ENST00000464097.5:n.269C>G (ADA)
ENST00000492931.5:n.679C>G (ADA)
ENST00000536532.5:c.595C>G (ADA)	ENSP00000440946.1:p.Gln199Glu
ENST00000537820.1:c.595C>G (ADA)	ENSP00000441818.1:p.Gln199Glu
ENST00000539235.5:c.219-1135C>G (ADA)	ENSP00000446464.1:n.219-1135C>G
NM_000022.2:c.595C>G , LRG_16t1:c.595C>G (ADA)	NP_000013.2:p.Gln199Glu
XM_005260236.2:c.595C>G (ADA)	XP_005260293.1:p.Gln199Glu
XM_011528478.1:c.190C>G (ADA)	XP_011526780.1:p.Gln64Glu
XM_011528479.1:c.190C>G (ADA)	XP_011526781.1:p.Gln64Glu
XR_244129.1:n.649C>G (ADA)
NM_000022.3:c.595C>G (ADA)	NP_000013.2:p.Gln199Glu
NM_001322050.1:c.190C>G (ADA)	NP_001308979.1:p.Gln64Glu
NM_001322051.1:c.595C>G (ADA)	NP_001308980.1:p.Gln199Glu
NR_136160.1:n.746C>G (ADA)
NM_000022.4:c.595C>G (ADA) MANE Select	NP_000013.2:p.Gln199Glu
NM_001322050.2:c.190C>G (ADA)	NP_001308979.1:p.Gln64Glu
NM_001322051.2:c.595C>G (ADA)	NP_001308980.1:p.Gln199Glu
NR_136160.2:n.687C>G (ADA)