Canonical Allele Identifier: CA409121396

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43255163T>A (hg19) ; chr20:g.44626522T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44626522T>A , CM000682.2:g.44626522T>A	GRCh38
NC_000020.10:g.43255163T>A , CM000682.1:g.43255163T>A	GRCh37
NC_000020.9:g.42688577T>A	NCBI36
NG_007385.1:g.30214A>T , LRG_16:g.30214A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.387A>T
ENST00000536076.2:c.143A>T	ENSP00000512234.1:p.Glu48Val
ENST00000536532.6:c.296A>T	ENSP00000440946.1:p.Glu99Val
ENST00000537820.2:c.296A>T	ENSP00000441818.1:p.Glu99Val
ENST00000539235.6:c.218+2525A>T	ENSP00000446464.1:n.218+2525A>T
ENST00000695889.1:c.218+2525A>T	ENSP00000512240.1:n.218+2525A>T
ENST00000695890.1:n.2099A>T
ENST00000695891.1:c.218+2525A>T	ENSP00000512241.1:n.218+2525A>T
ENST00000695927.1:c.374A>T	ENSP00000512270.1:p.Glu125Val
ENST00000695949.1:c.293A>T	ENSP00000512281.1:p.Glu98Val
ENST00000695957.1:c.296A>T	ENSP00000512286.1:p.Glu99Val
ENST00000695991.1:c.216+2527A>T	ENSP00000512314.1:n.216+2527A>T
ENST00000695992.1:c.296A>T	ENSP00000512315.1:p.Glu99Val
ENST00000695993.1:c.296A>T	ENSP00000512316.1:p.Glu99Val
ENST00000695994.1:c.296A>T	ENSP00000512317.1:p.Glu99Val
ENST00000695995.1:c.216+2527A>T	ENSP00000512318.1:n.216+2527A>T
ENST00000695996.1:n.367A>T
ENST00000695997.1:n.367A>T
ENST00000696003.1:n.388A>T
ENST00000696004.1:n.388A>T
ENST00000696006.1:c.296A>T	ENSP00000512325.1:p.Glu99Val
ENST00000696007.1:c.263A>T	ENSP00000512326.1:p.Glu88Val
ENST00000696009.1:n.407A>T
ENST00000696017.1:c.293A>T	ENSP00000512333.1:p.Glu98Val
ENST00000696034.1:c.296A>T	ENSP00000512343.1:p.Glu99Val
ENST00000696035.1:n.406A>T
ENST00000696036.1:n.986A>T
ENST00000696037.1:n.1973A>T
ENST00000696038.1:c.*42A>T	ENSP00000512344.1:n.*42A>T
ENST00000696039.1:n.584A>T
ENST00000696058.1:c.296A>T	ENSP00000512361.1:p.Glu99Val
ENST00000696059.1:c.*241A>T	ENSP00000512362.1:n.*241A>T
ENST00000696060.1:c.296A>T	ENSP00000512363.1:p.Glu99Val
ENST00000696061.1:c.293A>T	ENSP00000512364.1:p.Glu98Val
ENST00000696062.1:c.359A>T	ENSP00000512365.1:p.Glu120Val
ENST00000696063.1:c.371A>T	ENSP00000512366.1:p.Glu124Val
ENST00000696064.1:c.143A>T	ENSP00000512367.1:p.Glu48Val
ENST00000696065.1:c.65+2525A>T	ENSP00000512368.1:n.65+2525A>T
ENST00000696075.1:c.*266A>T	ENSP00000512374.1:n.*266A>T
ENST00000696076.1:c.296A>T	ENSP00000512375.1:p.Glu99Val
ENST00000696077.1:c.293A>T	ENSP00000512376.1:p.Glu98Val
ENST00000696078.1:c.296A>T	ENSP00000512377.1:p.Glu99Val
ENST00000696079.1:c.296A>T	ENSP00000512378.1:p.Glu99Val
ENST00000696080.1:c.296A>T	ENSP00000512379.1:p.Glu99Val
ENST00000696082.1:c.374A>T	ENSP00000512380.1:p.Glu125Val
ENST00000696084.1:n.397A>T
ENST00000696104.1:c.296A>T	ENSP00000512399.1:p.Glu99Val
ENST00000696105.1:c.296A>T	ENSP00000512400.1:p.Glu99Val
ENST00000372874.9:c.296A>T MANE Select	ENSP00000361965.4:p.Glu99Val
ENST00000372874.8:c.296A>T	ENSP00000361965.4:p.Glu99Val
ENST00000492931.5:n.380A>T
ENST00000536076.1:n.476A>T
ENST00000536532.5:c.296A>T	ENSP00000440946.1:p.Glu99Val
ENST00000537820.1:c.296A>T	ENSP00000441818.1:p.Glu99Val
ENST00000539235.5:c.218+2525A>T	ENSP00000446464.1:n.218+2525A>T
ENST00000545776.5:n.350A>T
NM_000022.2:c.296A>T , LRG_16t1:c.296A>T	NP_000013.2:p.Glu99Val
XM_005260236.2:c.296A>T	XP_005260293.1:p.Glu99Val
XM_011528478.1:c.7A>T	XP_011526780.1:p.Arg3Trp
XM_011528479.1:c.7A>T	XP_011526781.1:p.Arg3Trp
XR_244129.1:n.350A>T
NM_000022.3:c.296A>T	NP_000013.2:p.Glu99Val
NM_001322050.1:c.7A>T	NP_001308979.1:p.Arg3Trp
NM_001322051.1:c.296A>T	NP_001308980.1:p.Glu99Val
NR_136160.1:n.447A>T
NM_000022.4:c.296A>T MANE Select	NP_000013.2:p.Glu99Val
NM_001322050.2:c.7A>T	NP_001308979.1:p.Arg3Trp
NM_001322051.2:c.296A>T	NP_001308980.1:p.Glu99Val
NR_136160.2:n.388A>T