Canonical Allele Identifier: CA409120882

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43252914C>A (hg19) ; chr20:g.44624273C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44624273C>A , CM000682.2:g.44624273C>A	GRCh38
NC_000020.10:g.43252914C>A , CM000682.1:g.43252914C>A	GRCh37
NC_000020.9:g.42686328C>A	NCBI36
NG_007385.1:g.32463G>T , LRG_16:g.32463G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.626G>T
ENST00000536076.2:c.382G>T	ENSP00000512234.1:p.Ala128Ser
ENST00000536532.6:c.535G>T	ENSP00000440946.1:p.Ala179Ser
ENST00000537820.2:c.535G>T	ENSP00000441818.1:p.Ala179Ser
ENST00000539235.6:c.219-1195G>T	ENSP00000446464.1:n.219-1195G>T
ENST00000695889.1:c.219-1343G>T	ENSP00000512240.1:n.219-1343G>T
ENST00000695890.1:n.2338G>T
ENST00000695891.1:c.219-1343G>T	ENSP00000512241.1:n.219-1343G>T
ENST00000695927.1:c.613G>T	ENSP00000512270.1:p.Ala205Ser
ENST00000695949.1:c.532G>T	ENSP00000512281.1:p.Ala178Ser
ENST00000695957.1:c.*26G>T	ENSP00000512286.1:n.*26G>T
ENST00000695991.1:c.217-1343G>T	ENSP00000512314.1:n.217-1343G>T
ENST00000695992.1:c.535G>T	ENSP00000512315.1:p.Ala179Ser
ENST00000695993.1:c.535G>T	ENSP00000512316.1:p.Ala179Ser
ENST00000695994.1:c.535G>T	ENSP00000512317.1:p.Ala179Ser
ENST00000695995.1:c.217-1195G>T	ENSP00000512318.1:n.217-1195G>T
ENST00000695996.1:n.606G>T
ENST00000695997.1:n.490G>T
ENST00000696003.1:n.627G>T
ENST00000696004.1:n.627G>T
ENST00000696005.1:c.57G>T
ENST00000696006.1:c.535G>T	ENSP00000512325.1:p.Ala179Ser
ENST00000696007.1:c.386G>T	ENSP00000512326.1:n.386G>T
ENST00000696008.1:n.1690G>T
ENST00000696009.1:n.1885G>T
ENST00000696017.1:c.532G>T	ENSP00000512333.1:p.Ala178Ser
ENST00000696034.1:c.535G>T	ENSP00000512343.1:p.Ala179Ser
ENST00000696035.1:n.645G>T
ENST00000696036.1:n.1225G>T
ENST00000696037.1:n.2212G>T
ENST00000696038.1:c.*281G>T	ENSP00000512344.1:n.*281G>T
ENST00000696039.1:n.823G>T
ENST00000696058.1:c.535G>T	ENSP00000512361.1:p.Ala179Ser
ENST00000696059.1:c.*480G>T	ENSP00000512362.1:n.*480G>T
ENST00000696060.1:c.535G>T	ENSP00000512363.1:p.Ala179Ser
ENST00000696061.1:c.532G>T	ENSP00000512364.1:p.Ala178Ser
ENST00000696062.1:c.598G>T	ENSP00000512365.1:p.Ala200Ser
ENST00000696063.1:c.610G>T	ENSP00000512366.1:p.Ala204Ser
ENST00000696064.1:c.382G>T	ENSP00000512367.1:p.Ala128Ser
ENST00000696065.1:c.66-1343G>T	ENSP00000512368.1:n.66-1343G>T
ENST00000696074.1:n.151G>T
ENST00000696075.1:c.*505G>T	ENSP00000512374.1:n.*505G>T
ENST00000696076.1:c.535G>T	ENSP00000512375.1:p.Ala179Ser
ENST00000696077.1:c.532G>T	ENSP00000512376.1:p.Ala178Ser
ENST00000696078.1:c.535G>T	ENSP00000512377.1:p.Ala179Ser
ENST00000696079.1:c.535G>T	ENSP00000512378.1:p.Ala179Ser
ENST00000696080.1:c.535G>T	ENSP00000512379.1:p.Ala179Ser
ENST00000696081.1:n.654G>T
ENST00000696082.1:c.613G>T	ENSP00000512380.1:p.Ala205Ser
ENST00000696083.1:n.1416G>T
ENST00000696084.1:n.636G>T
ENST00000696104.1:c.363-1343G>T	ENSP00000512399.1:n.363-1343G>T
ENST00000696105.1:c.*76G>T	ENSP00000512400.1:n.*76G>T
ENST00000372874.9:c.535G>T MANE Select	ENSP00000361965.4:p.Ala179Ser
ENST00000372874.8:c.535G>T	ENSP00000361965.4:p.Ala179Ser
ENST00000464097.5:n.209G>T
ENST00000492931.5:n.619G>T
ENST00000536532.5:c.535G>T	ENSP00000440946.1:p.Ala179Ser
ENST00000537820.1:c.535G>T	ENSP00000441818.1:p.Ala179Ser
ENST00000539235.5:c.219-1195G>T	ENSP00000446464.1:n.219-1195G>T
NM_000022.2:c.535G>T , LRG_16t1:c.535G>T	NP_000013.2:p.Ala179Ser
XM_005260236.2:c.535G>T	XP_005260293.1:p.Ala179Ser
XM_011528478.1:c.130G>T	XP_011526780.1:p.Ala44Ser
XM_011528479.1:c.130G>T	XP_011526781.1:p.Ala44Ser
XR_244129.1:n.589G>T
NM_000022.3:c.535G>T	NP_000013.2:p.Ala179Ser
NM_001322050.1:c.130G>T	NP_001308979.1:p.Ala44Ser
NM_001322051.1:c.535G>T	NP_001308980.1:p.Ala179Ser
NR_136160.1:n.686G>T
NM_000022.4:c.535G>T MANE Select	NP_000013.2:p.Ala179Ser
NM_001322050.2:c.130G>T	NP_001308979.1:p.Ala44Ser
NM_001322051.2:c.535G>T	NP_001308980.1:p.Ala179Ser
NR_136160.2:n.627G>T