Canonical Allele Identifier: CA409120997

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43252967C>A (hg19) ; chr20:g.44624326C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44624326C>A , CM000682.2:g.44624326C>A	GRCh38
NC_000020.10:g.43252967C>A , CM000682.1:g.43252967C>A	GRCh37
NC_000020.9:g.42686381C>A	NCBI36
NG_007385.1:g.32410G>T , LRG_16:g.32410G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.573G>T
ENST00000536076.2:c.329G>T	ENSP00000512234.1:p.Trp110Leu
ENST00000536532.6:c.482G>T	ENSP00000440946.1:p.Trp161Leu
ENST00000537820.2:c.482G>T	ENSP00000441818.1:p.Trp161Leu
ENST00000539235.6:c.219-1248G>T	ENSP00000446464.1:n.219-1248G>T
ENST00000695889.1:c.219-1396G>T	ENSP00000512240.1:n.219-1396G>T
ENST00000695890.1:n.2285G>T
ENST00000695891.1:c.219-1396G>T	ENSP00000512241.1:n.219-1396G>T
ENST00000695927.1:c.560G>T	ENSP00000512270.1:p.Trp187Leu
ENST00000695949.1:c.479G>T	ENSP00000512281.1:p.Trp160Leu
ENST00000695957.1:c.366G>T	ENSP00000512286.1:p.Leu122=
ENST00000695991.1:c.217-1396G>T	ENSP00000512314.1:n.217-1396G>T
ENST00000695992.1:c.482G>T	ENSP00000512315.1:p.Trp161Leu
ENST00000695993.1:c.482G>T	ENSP00000512316.1:p.Trp161Leu
ENST00000695994.1:c.482G>T	ENSP00000512317.1:p.Trp161Leu
ENST00000695995.1:c.217-1248G>T	ENSP00000512318.1:n.217-1248G>T
ENST00000695996.1:n.553G>T
ENST00000695997.1:n.437G>T
ENST00000696003.1:n.574G>T
ENST00000696004.1:n.574G>T
ENST00000696005.1:c.4G>T
ENST00000696006.1:c.482G>T	ENSP00000512325.1:p.Trp161Leu
ENST00000696007.1:c.333G>T	ENSP00000512326.1:p.Leu111=
ENST00000696008.1:n.1637G>T
ENST00000696009.1:n.1832G>T
ENST00000696017.1:c.479G>T	ENSP00000512333.1:p.Trp160Leu
ENST00000696034.1:c.482G>T	ENSP00000512343.1:p.Trp161Leu
ENST00000696035.1:n.592G>T
ENST00000696036.1:n.1172G>T
ENST00000696037.1:n.2159G>T
ENST00000696038.1:c.*228G>T	ENSP00000512344.1:n.*228G>T
ENST00000696039.1:n.770G>T
ENST00000696058.1:c.482G>T	ENSP00000512361.1:p.Trp161Leu
ENST00000696059.1:c.*427G>T	ENSP00000512362.1:n.*427G>T
ENST00000696060.1:c.482G>T	ENSP00000512363.1:p.Trp161Leu
ENST00000696061.1:c.479G>T	ENSP00000512364.1:p.Trp160Leu
ENST00000696062.1:c.545G>T	ENSP00000512365.1:p.Trp182Leu
ENST00000696063.1:c.557G>T	ENSP00000512366.1:p.Trp186Leu
ENST00000696064.1:c.329G>T	ENSP00000512367.1:p.Trp110Leu
ENST00000696065.1:c.66-1396G>T	ENSP00000512368.1:n.66-1396G>T
ENST00000696074.1:n.98G>T
ENST00000696075.1:c.*452G>T	ENSP00000512374.1:n.*452G>T
ENST00000696076.1:c.482G>T	ENSP00000512375.1:p.Trp161Leu
ENST00000696077.1:c.479G>T	ENSP00000512376.1:p.Trp160Leu
ENST00000696078.1:c.482G>T	ENSP00000512377.1:p.Trp161Leu
ENST00000696079.1:c.482G>T	ENSP00000512378.1:p.Trp161Leu
ENST00000696080.1:c.482G>T	ENSP00000512379.1:p.Trp161Leu
ENST00000696081.1:n.601G>T
ENST00000696082.1:c.560G>T	ENSP00000512380.1:p.Trp187Leu
ENST00000696083.1:n.1363G>T
ENST00000696084.1:n.583G>T
ENST00000696104.1:c.363-1396G>T	ENSP00000512399.1:n.363-1396G>T
ENST00000696105.1:c.*23G>T	ENSP00000512400.1:n.*23G>T
ENST00000372874.9:c.482G>T MANE Select	ENSP00000361965.4:p.Trp161Leu
ENST00000372874.8:c.482G>T	ENSP00000361965.4:p.Trp161Leu
ENST00000464097.5:n.156G>T
ENST00000492931.5:n.566G>T
ENST00000536532.5:c.482G>T	ENSP00000440946.1:p.Trp161Leu
ENST00000537820.1:c.482G>T	ENSP00000441818.1:p.Trp161Leu
ENST00000539235.5:c.219-1248G>T	ENSP00000446464.1:n.219-1248G>T
NM_000022.2:c.482G>T , LRG_16t1:c.482G>T	NP_000013.2:p.Trp161Leu
XM_005260236.2:c.482G>T	XP_005260293.1:p.Trp161Leu
XM_011528478.1:c.77G>T	XP_011526780.1:p.Trp26Leu
XM_011528479.1:c.77G>T	XP_011526781.1:p.Trp26Leu
XR_244129.1:n.536G>T
NM_000022.3:c.482G>T	NP_000013.2:p.Trp161Leu
NM_001322050.1:c.77G>T	NP_001308979.1:p.Trp26Leu
NM_001322051.1:c.482G>T	NP_001308980.1:p.Trp161Leu
NR_136160.1:n.633G>T
NM_000022.4:c.482G>T MANE Select	NP_000013.2:p.Trp161Leu
NM_001322050.2:c.77G>T	NP_001308979.1:p.Trp26Leu
NM_001322051.2:c.482G>T	NP_001308980.1:p.Trp161Leu
NR_136160.2:n.574G>T