Canonical Allele Identifier: CA409121066

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43254231A>C (hg19) ; chr20:g.44625590A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44625590A>C , CM000682.2:g.44625590A>C	GRCh38
NC_000020.10:g.43254231A>C , CM000682.1:g.43254231A>C	GRCh37
NC_000020.9:g.42687645A>C	NCBI36
NG_007385.1:g.31146T>G , LRG_16:g.31146T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.548T>G
ENST00000536076.2:c.304T>G	ENSP00000512234.1:p.Cys102Gly
ENST00000536532.6:c.457T>G	ENSP00000440946.1:p.Cys153Gly
ENST00000537820.2:c.457T>G	ENSP00000441818.1:p.Cys153Gly
ENST00000539235.6:c.219-2512T>G	ENSP00000446464.1:n.219-2512T>G
ENST00000695889.1:c.219-2660T>G	ENSP00000512240.1:n.219-2660T>G
ENST00000695890.1:n.2260T>G
ENST00000695891.1:c.219-2660T>G	ENSP00000512241.1:n.219-2660T>G
ENST00000695927.1:c.535T>G	ENSP00000512270.1:p.Cys179Gly
ENST00000695949.1:c.454T>G	ENSP00000512281.1:p.Cys152Gly
ENST00000695957.1:c.362+866T>G	ENSP00000512286.1:n.362+866T>G
ENST00000695991.1:c.217-2660T>G	ENSP00000512314.1:n.217-2660T>G
ENST00000695992.1:c.457T>G	ENSP00000512315.1:p.Cys153Gly
ENST00000695993.1:c.457T>G	ENSP00000512316.1:p.Cys153Gly
ENST00000695994.1:c.457T>G	ENSP00000512317.1:p.Cys153Gly
ENST00000695995.1:c.217-2512T>G	ENSP00000512318.1:n.217-2512T>G
ENST00000695996.1:n.528T>G
ENST00000695997.1:n.433+866T>G
ENST00000696003.1:n.549T>G
ENST00000696004.1:n.549T>G
ENST00000696006.1:c.457T>G	ENSP00000512325.1:p.Cys153Gly
ENST00000696007.1:c.329+866T>G	ENSP00000512326.1:n.329+866T>G
ENST00000696008.1:n.373T>G
ENST00000696009.1:n.568T>G
ENST00000696017.1:c.454T>G	ENSP00000512333.1:p.Cys152Gly
ENST00000696034.1:c.457T>G	ENSP00000512343.1:p.Cys153Gly
ENST00000696035.1:n.567T>G
ENST00000696036.1:n.1147T>G
ENST00000696037.1:n.2134T>G
ENST00000696038.1:c.*203T>G	ENSP00000512344.1:n.*203T>G
ENST00000696039.1:n.745T>G
ENST00000696058.1:c.457T>G	ENSP00000512361.1:p.Cys153Gly
ENST00000696059.1:c.*402T>G	ENSP00000512362.1:n.*402T>G
ENST00000696060.1:c.457T>G	ENSP00000512363.1:p.Cys153Gly
ENST00000696061.1:c.454T>G	ENSP00000512364.1:p.Cys152Gly
ENST00000696062.1:c.520T>G	ENSP00000512365.1:p.Cys174Gly
ENST00000696063.1:c.532T>G	ENSP00000512366.1:p.Cys178Gly
ENST00000696064.1:c.304T>G	ENSP00000512367.1:p.Cys102Gly
ENST00000696065.1:c.66-2660T>G	ENSP00000512368.1:n.66-2660T>G
ENST00000696075.1:c.*427T>G	ENSP00000512374.1:n.*427T>G
ENST00000696076.1:c.457T>G	ENSP00000512375.1:p.Cys153Gly
ENST00000696077.1:c.454T>G	ENSP00000512376.1:p.Cys152Gly
ENST00000696078.1:c.457T>G	ENSP00000512377.1:p.Cys153Gly
ENST00000696079.1:c.457T>G	ENSP00000512378.1:p.Cys153Gly
ENST00000696080.1:c.457T>G	ENSP00000512379.1:p.Cys153Gly
ENST00000696082.1:c.535T>G	ENSP00000512380.1:p.Cys179Gly
ENST00000696083.1:n.99T>G
ENST00000696084.1:n.558T>G
ENST00000696104.1:c.362+866T>G	ENSP00000512399.1:n.362+866T>G
ENST00000696105.1:c.457T>G	ENSP00000512400.1:p.Cys153Gly
ENST00000372874.9:c.457T>G MANE Select	ENSP00000361965.4:p.Cys153Gly
ENST00000372874.8:c.457T>G	ENSP00000361965.4:p.Cys153Gly
ENST00000464097.5:n.131T>G
ENST00000492931.5:n.541T>G
ENST00000536532.5:c.457T>G	ENSP00000440946.1:p.Cys153Gly
ENST00000537820.1:c.457T>G	ENSP00000441818.1:p.Cys153Gly
ENST00000539235.5:c.219-2512T>G	ENSP00000446464.1:n.219-2512T>G
NM_000022.2:c.457T>G , LRG_16t1:c.457T>G	NP_000013.2:p.Cys153Gly
XM_005260236.2:c.457T>G	XP_005260293.1:p.Cys153Gly
XM_011528478.1:c.73+866T>G	XP_011526780.1:n.73+866T>G
XM_011528479.1:c.73+866T>G	XP_011526781.1:n.73+866T>G
XR_244129.1:n.511T>G
NM_000022.3:c.457T>G	NP_000013.2:p.Cys153Gly
NM_001322050.1:c.73+866T>G	NP_001308979.1:n.73+866T>G
NM_001322051.1:c.457T>G	NP_001308980.1:p.Cys153Gly
NR_136160.1:n.608T>G
NM_000022.4:c.457T>G MANE Select	NP_000013.2:p.Cys153Gly
NM_001322050.2:c.73+866T>G	NP_001308979.1:n.73+866T>G
NM_001322051.2:c.457T>G	NP_001308980.1:p.Cys153Gly
NR_136160.2:n.549T>G