Canonical Allele Identifier: CA409120290

Gene: ADA PKIG

Linked Data

• MyVariant Identifiers: chr20:g.43251537T>C (hg19) ; chr20:g.44622896T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44622896T>C , CM000682.2:g.44622896T>C	GRCh38
NC_000020.10:g.43251537T>C , CM000682.1:g.43251537T>C	GRCh37
NC_000020.9:g.42684951T>C	NCBI36
NG_007385.1:g.33840A>G , LRG_16:g.33840A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.880A>G (ADA)
ENST00000536076.2:c.560A>G (ADA)	ENSP00000512234.1:p.His187Arg
ENST00000536532.6:c.713A>G (ADA)	ENSP00000440946.1:p.His238Arg
ENST00000537820.2:c.641A>G (ADA)	ENSP00000441818.1:p.His214Arg
ENST00000539235.6:c.*97A>G (ADA)	ENSP00000446464.1:n.*97A>G
ENST00000695889.1:c.253A>G (ADA)	ENSP00000512240.1:p.Thr85Ala
ENST00000695890.1:n.2592A>G (ADA)
ENST00000695891.1:c.253A>G (ADA)	ENSP00000512241.1:p.Thr85Ala
ENST00000695927.1:c.791A>G (ADA)	ENSP00000512270.1:p.His264Arg
ENST00000695949.1:c.638A>G (ADA)	ENSP00000512281.1:p.His213Arg
ENST00000695957.1:c.*204A>G (ADA)	ENSP00000512286.1:n.*204A>G
ENST00000695991.1:c.251A>G (ADA)	ENSP00000512314.1:p.His84Arg
ENST00000695992.1:c.713A>G (ADA)	ENSP00000512315.1:p.His238Arg
ENST00000695993.1:c.713A>G (ADA)	ENSP00000512316.1:p.His238Arg
ENST00000695994.1:c.686A>G (ADA)	ENSP00000512317.1:p.His229Arg
ENST00000695995.1:c.323A>G (ADA)	ENSP00000512318.1:p.His108Arg
ENST00000695996.1:n.860A>G (ADA)
ENST00000696003.1:n.881A>G (ADA)
ENST00000696004.1:n.881A>G (ADA)
ENST00000696005.1:c.163A>G (ADA)
ENST00000696006.1:c.641A>G (ADA)	ENSP00000512325.1:p.His214Arg
ENST00000696007.1:c.640A>G (ADA)	ENSP00000512326.1:n.640A>G
ENST00000696008.1:n.3067A>G (ADA)
ENST00000696017.1:c.710A>G (ADA)	ENSP00000512333.1:p.His237Arg
ENST00000696034.1:c.713A>G (ADA)	ENSP00000512343.1:p.His238Arg
ENST00000696035.1:n.899A>G (ADA)
ENST00000696036.1:n.1479A>G (ADA)
ENST00000696037.1:n.2390A>G (ADA)
ENST00000696038.1:c.*535A>G (ADA)	ENSP00000512344.1:n.*535A>G
ENST00000696039.1:n.1077A>G (ADA)
ENST00000696058.1:c.710A>G (ADA)	ENSP00000512361.1:p.His237Arg
ENST00000696059.1:c.*658A>G (ADA)	ENSP00000512362.1:n.*658A>G
ENST00000696060.1:c.782A>G (ADA)	ENSP00000512363.1:p.His261Arg
ENST00000696061.1:c.710A>G (ADA)	ENSP00000512364.1:p.His237Arg
ENST00000696062.1:c.776A>G (ADA)	ENSP00000512365.1:p.His259Arg
ENST00000696063.1:c.788A>G (ADA)	ENSP00000512366.1:p.His263Arg
ENST00000696064.1:c.560A>G (ADA)	ENSP00000512367.1:p.His187Arg
ENST00000696065.1:c.100A>G (ADA)	ENSP00000512368.1:p.Thr34Ala
ENST00000696073.1:n.1024A>G (ADA)
ENST00000696074.1:n.329A>G (ADA)
ENST00000696075.1:c.*683A>G (ADA)	ENSP00000512374.1:n.*683A>G
ENST00000696076.1:c.782A>G (ADA)	ENSP00000512375.1:p.His261Arg
ENST00000696077.1:c.707A>G (ADA)	ENSP00000512376.1:p.His236Arg
ENST00000696078.1:c.710A>G (ADA)	ENSP00000512377.1:p.His237Arg
ENST00000696079.1:c.710A>G (ADA)	ENSP00000512378.1:p.His237Arg
ENST00000696080.1:c.713A>G (ADA)	ENSP00000512379.1:p.His238Arg
ENST00000696081.1:n.832A>G (ADA)
ENST00000696082.1:c.788A>G (ADA)	ENSP00000512380.1:p.His263Arg
ENST00000696083.1:n.1670A>G (ADA)
ENST00000696084.1:n.890A>G (ADA)
ENST00000696104.1:c.397A>G (ADA)	ENSP00000512399.1:p.Thr133Ala
ENST00000372874.9:c.713A>G (ADA) MANE Select	ENSP00000361965.4:p.His238Arg
ENST00000372874.8:c.713A>G (ADA)	ENSP00000361965.4:p.His238Arg
ENST00000372887.5:c.152-1037T>C (PKIG)	ENSP00000361978.1:n.152-1037T>C
ENST00000464097.5:n.463A>G (ADA)
ENST00000492931.5:n.873A>G (ADA)
ENST00000536532.5:c.713A>G (ADA)	ENSP00000440946.1:p.His238Arg
ENST00000537820.1:c.641A>G (ADA)	ENSP00000441818.1:p.His214Arg
ENST00000539235.5:c.*97A>G (ADA)	ENSP00000446464.1:n.*97A>G
NM_000022.2:c.713A>G , LRG_16t1:c.713A>G (ADA)	NP_000013.2:p.His238Arg
XM_005260236.2:c.641A>G (ADA)	XP_005260293.1:p.His214Arg
XM_011528478.1:c.308A>G (ADA)	XP_011526780.1:p.His103Arg
XM_011528479.1:c.308A>G (ADA)	XP_011526781.1:p.His103Arg
XR_244129.1:n.767A>G (ADA)
NM_000022.3:c.713A>G (ADA)	NP_000013.2:p.His238Arg
NM_001322050.1:c.308A>G (ADA)	NP_001308979.1:p.His103Arg
NM_001322051.1:c.641A>G (ADA)	NP_001308980.1:p.His214Arg
NR_136160.1:n.864A>G (ADA)
NM_000022.4:c.713A>G (ADA) MANE Select	NP_000013.2:p.His238Arg
NM_001322050.2:c.308A>G (ADA)	NP_001308979.1:p.His103Arg
NM_001322051.2:c.641A>G (ADA)	NP_001308980.1:p.His214Arg
NR_136160.2:n.805A>G (ADA)