Canonical Allele Identifier: CA409121280

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43255104G>C (hg19) ; chr20:g.44626463G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44626463G>C , CM000682.2:g.44626463G>C	GRCh38
NC_000020.10:g.43255104G>C , CM000682.1:g.43255104G>C	GRCh37
NC_000020.9:g.42688518G>C	NCBI36
NG_007385.1:g.30273C>G , LRG_16:g.30273C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.446C>G
ENST00000536076.2:c.202C>G	ENSP00000512234.1:p.Gln68Glu
ENST00000536532.6:c.355C>G	ENSP00000440946.1:p.Gln119Glu
ENST00000537820.2:c.355C>G	ENSP00000441818.1:p.Gln119Glu
ENST00000539235.6:c.218+2584C>G	ENSP00000446464.1:n.218+2584C>G
ENST00000695889.1:c.218+2584C>G	ENSP00000512240.1:n.218+2584C>G
ENST00000695890.1:n.2158C>G
ENST00000695891.1:c.218+2584C>G	ENSP00000512241.1:n.218+2584C>G
ENST00000695927.1:c.433C>G	ENSP00000512270.1:p.Gln145Glu
ENST00000695949.1:c.352C>G	ENSP00000512281.1:p.Gln118Glu
ENST00000695957.1:c.355C>G	ENSP00000512286.1:p.Gln119Glu
ENST00000695991.1:c.216+2586C>G	ENSP00000512314.1:n.216+2586C>G
ENST00000695992.1:c.355C>G	ENSP00000512315.1:p.Gln119Glu
ENST00000695993.1:c.355C>G	ENSP00000512316.1:p.Gln119Glu
ENST00000695994.1:c.355C>G	ENSP00000512317.1:p.Gln119Glu
ENST00000695995.1:c.216+2586C>G	ENSP00000512318.1:n.216+2586C>G
ENST00000695996.1:n.426C>G
ENST00000695997.1:n.426C>G
ENST00000696003.1:n.447C>G
ENST00000696004.1:n.447C>G
ENST00000696006.1:c.355C>G	ENSP00000512325.1:p.Gln119Glu
ENST00000696007.1:c.322C>G	ENSP00000512326.1:p.Gln108Glu
ENST00000696009.1:n.466C>G
ENST00000696017.1:c.352C>G	ENSP00000512333.1:p.Gln118Glu
ENST00000696034.1:c.355C>G	ENSP00000512343.1:p.Gln119Glu
ENST00000696035.1:n.465C>G
ENST00000696036.1:n.1045C>G
ENST00000696037.1:n.2032C>G
ENST00000696038.1:c.*101C>G	ENSP00000512344.1:n.*101C>G
ENST00000696039.1:n.643C>G
ENST00000696058.1:c.355C>G	ENSP00000512361.1:p.Gln119Glu
ENST00000696059.1:c.*300C>G	ENSP00000512362.1:n.*300C>G
ENST00000696060.1:c.355C>G	ENSP00000512363.1:p.Gln119Glu
ENST00000696061.1:c.352C>G	ENSP00000512364.1:p.Gln118Glu
ENST00000696062.1:c.418C>G	ENSP00000512365.1:p.Gln140Glu
ENST00000696063.1:c.430C>G	ENSP00000512366.1:p.Gln144Glu
ENST00000696064.1:c.202C>G	ENSP00000512367.1:p.Gln68Glu
ENST00000696065.1:c.65+2584C>G	ENSP00000512368.1:n.65+2584C>G
ENST00000696075.1:c.*325C>G	ENSP00000512374.1:n.*325C>G
ENST00000696076.1:c.355C>G	ENSP00000512375.1:p.Gln119Glu
ENST00000696077.1:c.352C>G	ENSP00000512376.1:p.Gln118Glu
ENST00000696078.1:c.355C>G	ENSP00000512377.1:p.Gln119Glu
ENST00000696079.1:c.355C>G	ENSP00000512378.1:p.Gln119Glu
ENST00000696080.1:c.355C>G	ENSP00000512379.1:p.Gln119Glu
ENST00000696082.1:c.433C>G	ENSP00000512380.1:p.Gln145Glu
ENST00000696084.1:n.456C>G
ENST00000696104.1:c.355C>G	ENSP00000512399.1:p.Gln119Glu
ENST00000696105.1:c.355C>G	ENSP00000512400.1:p.Gln119Glu
ENST00000372874.9:c.355C>G MANE Select	ENSP00000361965.4:p.Gln119Glu
ENST00000372874.8:c.355C>G	ENSP00000361965.4:p.Gln119Glu
ENST00000464097.5:n.29C>G
ENST00000492931.5:n.439C>G
ENST00000536532.5:c.355C>G	ENSP00000440946.1:p.Gln119Glu
ENST00000537820.1:c.355C>G	ENSP00000441818.1:p.Gln119Glu
ENST00000539235.5:c.218+2584C>G	ENSP00000446464.1:n.218+2584C>G
ENST00000545776.5:n.409C>G
NM_000022.2:c.355C>G , LRG_16t1:c.355C>G	NP_000013.2:p.Gln119Glu
XM_005260236.2:c.355C>G	XP_005260293.1:p.Gln119Glu
XM_011528478.1:c.66C>G	XP_011526780.1:p.Thr22=
XM_011528479.1:c.66C>G	XP_011526781.1:p.Thr22=
XR_244129.1:n.409C>G
NM_000022.3:c.355C>G	NP_000013.2:p.Gln119Glu
NM_001322050.1:c.66C>G	NP_001308979.1:p.Thr22=
NM_001322051.1:c.355C>G	NP_001308980.1:p.Gln119Glu
NR_136160.1:n.506C>G
NM_000022.4:c.355C>G MANE Select	NP_000013.2:p.Gln119Glu
NM_001322050.2:c.66C>G	NP_001308979.1:p.Thr22=
NM_001322051.2:c.355C>G	NP_001308980.1:p.Gln119Glu
NR_136160.2:n.447C>G