Canonical Allele Identifier: CA409121067

Gene: ADA

Linked Data

• gnomAD v4: 20-44625590-A-G
• MyVariant Identifiers: chr20:g.43254231A>G (hg19) ; chr20:g.44625590A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.548T>C
ENST00000536076.2:c.304T>C	ENSP00000512234.1:p.Cys102Arg
ENST00000536532.6:c.457T>C	ENSP00000440946.1:p.Cys153Arg
ENST00000537820.2:c.457T>C	ENSP00000441818.1:p.Cys153Arg
ENST00000539235.6:c.219-2512T>C	ENSP00000446464.1:n.219-2512T>C
ENST00000695889.1:c.219-2660T>C	ENSP00000512240.1:n.219-2660T>C
ENST00000695890.1:n.2260T>C
ENST00000695891.1:c.219-2660T>C	ENSP00000512241.1:n.219-2660T>C
ENST00000695927.1:c.535T>C	ENSP00000512270.1:p.Cys179Arg
ENST00000695949.1:c.454T>C	ENSP00000512281.1:p.Cys152Arg
ENST00000695957.1:c.362+866T>C	ENSP00000512286.1:n.362+866T>C
ENST00000695991.1:c.217-2660T>C	ENSP00000512314.1:n.217-2660T>C
ENST00000695992.1:c.457T>C	ENSP00000512315.1:p.Cys153Arg
ENST00000695993.1:c.457T>C	ENSP00000512316.1:p.Cys153Arg
ENST00000695994.1:c.457T>C	ENSP00000512317.1:p.Cys153Arg
ENST00000695995.1:c.217-2512T>C	ENSP00000512318.1:n.217-2512T>C
ENST00000695996.1:n.528T>C
ENST00000695997.1:n.433+866T>C
ENST00000696003.1:n.549T>C
ENST00000696004.1:n.549T>C
ENST00000696006.1:c.457T>C	ENSP00000512325.1:p.Cys153Arg
ENST00000696007.1:c.329+866T>C	ENSP00000512326.1:n.329+866T>C
ENST00000696008.1:n.373T>C
ENST00000696009.1:n.568T>C
ENST00000696017.1:c.454T>C	ENSP00000512333.1:p.Cys152Arg
ENST00000696034.1:c.457T>C	ENSP00000512343.1:p.Cys153Arg
ENST00000696035.1:n.567T>C
ENST00000696036.1:n.1147T>C
ENST00000696037.1:n.2134T>C
ENST00000696038.1:c.*203T>C	ENSP00000512344.1:n.*203T>C
ENST00000696039.1:n.745T>C
ENST00000696058.1:c.457T>C	ENSP00000512361.1:p.Cys153Arg
ENST00000696059.1:c.*402T>C	ENSP00000512362.1:n.*402T>C
ENST00000696060.1:c.457T>C	ENSP00000512363.1:p.Cys153Arg
ENST00000696061.1:c.454T>C	ENSP00000512364.1:p.Cys152Arg
ENST00000696062.1:c.520T>C	ENSP00000512365.1:p.Cys174Arg
ENST00000696063.1:c.532T>C	ENSP00000512366.1:p.Cys178Arg
ENST00000696064.1:c.304T>C	ENSP00000512367.1:p.Cys102Arg
ENST00000696065.1:c.66-2660T>C	ENSP00000512368.1:n.66-2660T>C
ENST00000696075.1:c.*427T>C	ENSP00000512374.1:n.*427T>C
ENST00000696076.1:c.457T>C	ENSP00000512375.1:p.Cys153Arg
ENST00000696077.1:c.454T>C	ENSP00000512376.1:p.Cys152Arg
ENST00000696078.1:c.457T>C	ENSP00000512377.1:p.Cys153Arg
ENST00000696079.1:c.457T>C	ENSP00000512378.1:p.Cys153Arg
ENST00000696080.1:c.457T>C	ENSP00000512379.1:p.Cys153Arg
ENST00000696082.1:c.535T>C	ENSP00000512380.1:p.Cys179Arg
ENST00000696083.1:n.99T>C
ENST00000696084.1:n.558T>C
ENST00000696104.1:c.362+866T>C	ENSP00000512399.1:n.362+866T>C
ENST00000696105.1:c.457T>C	ENSP00000512400.1:p.Cys153Arg
ENST00000372874.9:c.457T>C MANE Select	ENSP00000361965.4:p.Cys153Arg
ENST00000372874.8:c.457T>C	ENSP00000361965.4:p.Cys153Arg
ENST00000464097.5:n.131T>C
ENST00000492931.5:n.541T>C
ENST00000536532.5:c.457T>C	ENSP00000440946.1:p.Cys153Arg
ENST00000537820.1:c.457T>C	ENSP00000441818.1:p.Cys153Arg
ENST00000539235.5:c.219-2512T>C	ENSP00000446464.1:n.219-2512T>C
NM_000022.2:c.457T>C , LRG_16t1:c.457T>C	NP_000013.2:p.Cys153Arg
XM_005260236.2:c.457T>C	XP_005260293.1:p.Cys153Arg
XM_011528478.1:c.73+866T>C	XP_011526780.1:n.73+866T>C
XM_011528479.1:c.73+866T>C	XP_011526781.1:n.73+866T>C
XR_244129.1:n.511T>C
NM_000022.3:c.457T>C	NP_000013.2:p.Cys153Arg
NM_001322050.1:c.73+866T>C	NP_001308979.1:n.73+866T>C
NM_001322051.1:c.457T>C	NP_001308980.1:p.Cys153Arg
NR_136160.1:n.608T>C
NM_000022.4:c.457T>C MANE Select	NP_000013.2:p.Cys153Arg
NM_001322050.2:c.73+866T>C	NP_001308979.1:n.73+866T>C
NM_001322051.2:c.457T>C	NP_001308980.1:p.Cys153Arg
NR_136160.2:n.549T>C