Canonical Allele Identifier: CA409120963

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43252952A>C (hg19) ; chr20:g.44624311A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44624311A>C , CM000682.2:g.44624311A>C	GRCh38
NC_000020.10:g.43252952A>C , CM000682.1:g.43252952A>C	GRCh37
NC_000020.9:g.42686366A>C	NCBI36
NG_007385.1:g.32425T>G , LRG_16:g.32425T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.588T>G
ENST00000536076.2:c.344T>G	ENSP00000512234.1:p.Val115Gly
ENST00000536532.6:c.497T>G	ENSP00000440946.1:p.Val166Gly
ENST00000537820.2:c.497T>G	ENSP00000441818.1:p.Val166Gly
ENST00000539235.6:c.219-1233T>G	ENSP00000446464.1:n.219-1233T>G
ENST00000695889.1:c.219-1381T>G	ENSP00000512240.1:n.219-1381T>G
ENST00000695890.1:n.2300T>G
ENST00000695891.1:c.219-1381T>G	ENSP00000512241.1:n.219-1381T>G
ENST00000695927.1:c.575T>G	ENSP00000512270.1:p.Val192Gly
ENST00000695949.1:c.494T>G	ENSP00000512281.1:p.Val165Gly
ENST00000695957.1:c.381T>G	ENSP00000512286.1:p.Gly127=
ENST00000695991.1:c.217-1381T>G	ENSP00000512314.1:n.217-1381T>G
ENST00000695992.1:c.497T>G	ENSP00000512315.1:p.Val166Gly
ENST00000695993.1:c.497T>G	ENSP00000512316.1:p.Val166Gly
ENST00000695994.1:c.497T>G	ENSP00000512317.1:p.Val166Gly
ENST00000695995.1:c.217-1233T>G	ENSP00000512318.1:n.217-1233T>G
ENST00000695996.1:n.568T>G
ENST00000695997.1:n.452T>G
ENST00000696003.1:n.589T>G
ENST00000696004.1:n.589T>G
ENST00000696005.1:c.19T>G
ENST00000696006.1:c.497T>G	ENSP00000512325.1:p.Val166Gly
ENST00000696007.1:c.348T>G	ENSP00000512326.1:p.Gly116=
ENST00000696008.1:n.1652T>G
ENST00000696009.1:n.1847T>G
ENST00000696017.1:c.494T>G	ENSP00000512333.1:p.Val165Gly
ENST00000696034.1:c.497T>G	ENSP00000512343.1:p.Val166Gly
ENST00000696035.1:n.607T>G
ENST00000696036.1:n.1187T>G
ENST00000696037.1:n.2174T>G
ENST00000696038.1:c.*243T>G	ENSP00000512344.1:n.*243T>G
ENST00000696039.1:n.785T>G
ENST00000696058.1:c.497T>G	ENSP00000512361.1:p.Val166Gly
ENST00000696059.1:c.*442T>G	ENSP00000512362.1:n.*442T>G
ENST00000696060.1:c.497T>G	ENSP00000512363.1:p.Val166Gly
ENST00000696061.1:c.494T>G	ENSP00000512364.1:p.Val165Gly
ENST00000696062.1:c.560T>G	ENSP00000512365.1:p.Val187Gly
ENST00000696063.1:c.572T>G	ENSP00000512366.1:p.Val191Gly
ENST00000696064.1:c.344T>G	ENSP00000512367.1:p.Val115Gly
ENST00000696065.1:c.66-1381T>G	ENSP00000512368.1:n.66-1381T>G
ENST00000696074.1:n.113T>G
ENST00000696075.1:c.*467T>G	ENSP00000512374.1:n.*467T>G
ENST00000696076.1:c.497T>G	ENSP00000512375.1:p.Val166Gly
ENST00000696077.1:c.494T>G	ENSP00000512376.1:p.Val165Gly
ENST00000696078.1:c.497T>G	ENSP00000512377.1:p.Val166Gly
ENST00000696079.1:c.497T>G	ENSP00000512378.1:p.Val166Gly
ENST00000696080.1:c.497T>G	ENSP00000512379.1:p.Val166Gly
ENST00000696081.1:n.616T>G
ENST00000696082.1:c.575T>G	ENSP00000512380.1:p.Val192Gly
ENST00000696083.1:n.1378T>G
ENST00000696084.1:n.598T>G
ENST00000696104.1:c.363-1381T>G	ENSP00000512399.1:n.363-1381T>G
ENST00000696105.1:c.*38T>G	ENSP00000512400.1:n.*38T>G
ENST00000372874.9:c.497T>G MANE Select	ENSP00000361965.4:p.Val166Gly
ENST00000372874.8:c.497T>G	ENSP00000361965.4:p.Val166Gly
ENST00000464097.5:n.171T>G
ENST00000492931.5:n.581T>G
ENST00000536532.5:c.497T>G	ENSP00000440946.1:p.Val166Gly
ENST00000537820.1:c.497T>G	ENSP00000441818.1:p.Val166Gly
ENST00000539235.5:c.219-1233T>G	ENSP00000446464.1:n.219-1233T>G
NM_000022.2:c.497T>G , LRG_16t1:c.497T>G	NP_000013.2:p.Val166Gly
XM_005260236.2:c.497T>G	XP_005260293.1:p.Val166Gly
XM_011528478.1:c.92T>G	XP_011526780.1:p.Val31Gly
XM_011528479.1:c.92T>G	XP_011526781.1:p.Val31Gly
XR_244129.1:n.551T>G
NM_000022.3:c.497T>G	NP_000013.2:p.Val166Gly
NM_001322050.1:c.92T>G	NP_001308979.1:p.Val31Gly
NM_001322051.1:c.497T>G	NP_001308980.1:p.Val166Gly
NR_136160.1:n.648T>G
NM_000022.4:c.497T>G MANE Select	NP_000013.2:p.Val166Gly
NM_001322050.2:c.92T>G	NP_001308979.1:p.Val31Gly
NM_001322051.2:c.497T>G	NP_001308980.1:p.Val166Gly
NR_136160.2:n.589T>G