Canonical Allele Identifier: CA409120436

Gene: ADA PKIG

Linked Data

• MyVariant Identifiers: chr20:g.43251679C>G (hg19) ; chr20:g.44623038C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44623038C>G , CM000682.2:g.44623038C>G	GRCh38
NC_000020.10:g.43251679C>G , CM000682.1:g.43251679C>G	GRCh37
NC_000020.9:g.42685093C>G	NCBI36
NG_007385.1:g.33698G>C , LRG_16:g.33698G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.738G>C (ADA)
ENST00000536076.2:c.494G>C (ADA)	ENSP00000512234.1:p.Gly165Ala
ENST00000536532.6:c.647G>C (ADA)	ENSP00000440946.1:p.Gly216Ala
ENST00000537820.2:c.607-108G>C (ADA)	ENSP00000441818.1:n.607-108G>C
ENST00000539235.6:c.*31G>C (ADA)	ENSP00000446464.1:n.*31G>C
ENST00000695889.1:c.219-108G>C (ADA)	ENSP00000512240.1:n.219-108G>C
ENST00000695890.1:n.2450G>C (ADA)
ENST00000695891.1:c.219-108G>C (ADA)	ENSP00000512241.1:n.219-108G>C
ENST00000695927.1:c.725G>C (ADA)	ENSP00000512270.1:p.Gly242Ala
ENST00000695949.1:c.604-108G>C (ADA)	ENSP00000512281.1:n.604-108G>C
ENST00000695957.1:c.*138G>C (ADA)	ENSP00000512286.1:n.*138G>C
ENST00000695991.1:c.217-108G>C (ADA)	ENSP00000512314.1:n.217-108G>C
ENST00000695992.1:c.647G>C (ADA)	ENSP00000512315.1:p.Gly216Ala
ENST00000695993.1:c.647G>C (ADA)	ENSP00000512316.1:p.Gly216Ala
ENST00000695994.1:c.647G>C (ADA)	ENSP00000512317.1:p.Gly216Ala
ENST00000695995.1:c.257G>C (ADA)	ENSP00000512318.1:p.Gly86Ala
ENST00000695996.1:n.718G>C (ADA)
ENST00000696003.1:n.739G>C (ADA)
ENST00000696004.1:n.739G>C (ADA)
ENST00000696005.1:c.129-108G>C (ADA)
ENST00000696006.1:c.607-108G>C (ADA)	ENSP00000512325.1:n.607-108G>C
ENST00000696007.1:c.498G>C (ADA)	ENSP00000512326.1:n.498G>C
ENST00000696008.1:n.2925G>C (ADA)
ENST00000696017.1:c.644G>C (ADA)	ENSP00000512333.1:p.Gly215Ala
ENST00000696034.1:c.647G>C (ADA)	ENSP00000512343.1:p.Gly216Ala
ENST00000696035.1:n.757G>C (ADA)
ENST00000696036.1:n.1337G>C (ADA)
ENST00000696037.1:n.2324G>C (ADA)
ENST00000696038.1:c.*393G>C (ADA)	ENSP00000512344.1:n.*393G>C
ENST00000696039.1:n.935G>C (ADA)
ENST00000696058.1:c.644G>C (ADA)	ENSP00000512361.1:p.Gly215Ala
ENST00000696059.1:c.*592G>C (ADA)	ENSP00000512362.1:n.*592G>C
ENST00000696060.1:c.716G>C (ADA)	ENSP00000512363.1:p.Gly239Ala
ENST00000696061.1:c.644G>C (ADA)	ENSP00000512364.1:p.Gly215Ala
ENST00000696062.1:c.710G>C (ADA)	ENSP00000512365.1:p.Gly237Ala
ENST00000696063.1:c.722G>C (ADA)	ENSP00000512366.1:p.Gly241Ala
ENST00000696064.1:c.494G>C (ADA)	ENSP00000512367.1:p.Gly165Ala
ENST00000696065.1:c.66-108G>C (ADA)	ENSP00000512368.1:n.66-108G>C
ENST00000696073.1:n.882G>C (ADA)
ENST00000696074.1:n.263G>C (ADA)
ENST00000696075.1:c.*617G>C (ADA)	ENSP00000512374.1:n.*617G>C
ENST00000696076.1:c.716G>C (ADA)	ENSP00000512375.1:p.Gly239Ala
ENST00000696077.1:c.641G>C (ADA)	ENSP00000512376.1:p.Gly214Ala
ENST00000696078.1:c.644G>C (ADA)	ENSP00000512377.1:p.Gly215Ala
ENST00000696079.1:c.644G>C (ADA)	ENSP00000512378.1:p.Gly215Ala
ENST00000696080.1:c.647G>C (ADA)	ENSP00000512379.1:p.Gly216Ala
ENST00000696081.1:n.766G>C (ADA)
ENST00000696082.1:c.722G>C (ADA)	ENSP00000512380.1:p.Gly241Ala
ENST00000696083.1:n.1528G>C (ADA)
ENST00000696084.1:n.748G>C (ADA)
ENST00000696104.1:c.363-108G>C (ADA)	ENSP00000512399.1:n.363-108G>C
ENST00000696105.1:c.*188G>C (ADA)	ENSP00000512400.1:n.*188G>C
ENST00000372874.9:c.647G>C (ADA) MANE Select	ENSP00000361965.4:p.Gly216Ala
ENST00000372874.8:c.647G>C (ADA)	ENSP00000361965.4:p.Gly216Ala
ENST00000372887.5:c.152-895C>G (PKIG)	ENSP00000361978.1:n.152-895C>G
ENST00000464097.5:n.321G>C (ADA)
ENST00000492931.5:n.731G>C (ADA)
ENST00000536532.5:c.647G>C (ADA)	ENSP00000440946.1:p.Gly216Ala
ENST00000537820.1:c.607-108G>C (ADA)	ENSP00000441818.1:n.607-108G>C
ENST00000539235.5:c.*31G>C (ADA)	ENSP00000446464.1:n.*31G>C
NM_000022.2:c.647G>C , LRG_16t1:c.647G>C (ADA)	NP_000013.2:p.Gly216Ala
XM_005260236.2:c.607-108G>C (ADA)	XP_005260293.1:n.607-108G>C
XM_011528478.1:c.242G>C (ADA)	XP_011526780.1:p.Gly81Ala
XM_011528479.1:c.242G>C (ADA)	XP_011526781.1:p.Gly81Ala
XR_244129.1:n.701G>C (ADA)
NM_000022.3:c.647G>C (ADA)	NP_000013.2:p.Gly216Ala
NM_001322050.1:c.242G>C (ADA)	NP_001308979.1:p.Gly81Ala
NM_001322051.1:c.607-108G>C (ADA)	NP_001308980.1:n.607-108G>C
NR_136160.1:n.798G>C (ADA)
NM_000022.4:c.647G>C (ADA) MANE Select	NP_000013.2:p.Gly216Ala
NM_001322050.2:c.242G>C (ADA)	NP_001308979.1:p.Gly81Ala
NM_001322051.2:c.607-108G>C (ADA)	NP_001308980.1:n.607-108G>C
NR_136160.2:n.739G>C (ADA)