Canonical Allele Identifier: CA2838293914

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44624376A>G , CM000682.2:g.44624376A>G	GRCh38
NC_000020.10:g.43253017A>G , CM000682.1:g.43253017A>G	GRCh37
NC_000020.9:g.42686431A>G	NCBI36
NG_007385.1:g.32360T>C , LRG_16:g.32360T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.570-47T>C
ENST00000536076.2:c.326-47T>C	ENSP00000512234.1:n.326-47T>C
ENST00000536532.6:c.479-47T>C	ENSP00000440946.1:n.479-47T>C
ENST00000537820.2:c.479-47T>C	ENSP00000441818.1:n.479-47T>C
ENST00000539235.6:c.219-1298T>C	ENSP00000446464.1:n.219-1298T>C
ENST00000695889.1:c.219-1446T>C	ENSP00000512240.1:n.219-1446T>C
ENST00000695890.1:n.2282-47T>C
ENST00000695891.1:c.219-1446T>C	ENSP00000512241.1:n.219-1446T>C
ENST00000695927.1:c.557-47T>C	ENSP00000512270.1:n.557-47T>C
ENST00000695949.1:c.476-47T>C	ENSP00000512281.1:n.476-47T>C
ENST00000695957.1:c.363-47T>C	ENSP00000512286.1:n.363-47T>C
ENST00000695991.1:c.217-1446T>C	ENSP00000512314.1:n.217-1446T>C
ENST00000695992.1:c.479-47T>C	ENSP00000512315.1:n.479-47T>C
ENST00000695993.1:c.479-47T>C	ENSP00000512316.1:n.479-47T>C
ENST00000695994.1:c.479-47T>C	ENSP00000512317.1:n.479-47T>C
ENST00000695995.1:c.217-1298T>C	ENSP00000512318.1:n.217-1298T>C
ENST00000695996.1:n.550-47T>C
ENST00000695997.1:n.434-47T>C
ENST00000696003.1:n.571-47T>C
ENST00000696004.1:n.571-47T>C
ENST00000696006.1:c.479-47T>C	ENSP00000512325.1:n.479-47T>C
ENST00000696007.1:c.330-47T>C	ENSP00000512326.1:n.330-47T>C
ENST00000696008.1:n.1587T>C
ENST00000696009.1:n.1782T>C
ENST00000696017.1:c.476-47T>C	ENSP00000512333.1:n.476-47T>C
ENST00000696034.1:c.479-47T>C	ENSP00000512343.1:n.479-47T>C
ENST00000696035.1:n.589-47T>C
ENST00000696036.1:n.1169-47T>C
ENST00000696037.1:n.2156-47T>C
ENST00000696038.1:c.*225-47T>C	ENSP00000512344.1:n.*225-47T>C
ENST00000696039.1:n.767-47T>C
ENST00000696058.1:c.479-47T>C	ENSP00000512361.1:n.479-47T>C
ENST00000696059.1:c.*424-47T>C	ENSP00000512362.1:n.*424-47T>C
ENST00000696060.1:c.479-47T>C	ENSP00000512363.1:n.479-47T>C
ENST00000696061.1:c.476-47T>C	ENSP00000512364.1:n.476-47T>C
ENST00000696062.1:c.542-47T>C	ENSP00000512365.1:n.542-47T>C
ENST00000696063.1:c.554-47T>C	ENSP00000512366.1:n.554-47T>C
ENST00000696064.1:c.326-47T>C	ENSP00000512367.1:n.326-47T>C
ENST00000696065.1:c.66-1446T>C	ENSP00000512368.1:n.66-1446T>C
ENST00000696074.1:n.48T>C
ENST00000696075.1:c.*449-47T>C	ENSP00000512374.1:n.*449-47T>C
ENST00000696076.1:c.479-47T>C	ENSP00000512375.1:n.479-47T>C
ENST00000696077.1:c.476-47T>C	ENSP00000512376.1:n.476-47T>C
ENST00000696078.1:c.479-47T>C	ENSP00000512377.1:n.479-47T>C
ENST00000696079.1:c.479-47T>C	ENSP00000512378.1:n.479-47T>C
ENST00000696080.1:c.479-47T>C	ENSP00000512379.1:n.479-47T>C
ENST00000696081.1:n.551T>C
ENST00000696082.1:c.557-47T>C	ENSP00000512380.1:n.557-47T>C
ENST00000696083.1:n.1313T>C
ENST00000696084.1:n.580-47T>C
ENST00000696104.1:c.363-1446T>C	ENSP00000512399.1:n.363-1446T>C
ENST00000696105.1:c.*20-47T>C	ENSP00000512400.1:n.*20-47T>C
ENST00000372874.9:c.479-47T>C MANE Select	ENSP00000361965.4:n.479-47T>C
ENST00000372874.8:c.479-47T>C	ENSP00000361965.4:n.479-47T>C
ENST00000464097.5:n.153-47T>C
ENST00000492931.5:n.563-47T>C
ENST00000536532.5:c.479-47T>C	ENSP00000440946.1:n.479-47T>C
ENST00000537820.1:c.479-47T>C	ENSP00000441818.1:n.479-47T>C
ENST00000539235.5:c.219-1298T>C	ENSP00000446464.1:n.219-1298T>C
NM_000022.2:c.479-47T>C , LRG_16t1:c.479-47T>C	NP_000013.2:n.479-47T>C
XM_005260236.2:c.479-47T>C	XP_005260293.1:n.479-47T>C
XM_011528478.1:c.74-47T>C	XP_011526780.1:n.74-47T>C
XM_011528479.1:c.74-47T>C	XP_011526781.1:n.74-47T>C
XR_244129.1:n.533-47T>C
NM_000022.3:c.479-47T>C	NP_000013.2:n.479-47T>C
NM_001322050.1:c.74-47T>C	NP_001308979.1:n.74-47T>C
NM_001322051.1:c.479-47T>C	NP_001308980.1:n.479-47T>C
NR_136160.1:n.630-47T>C
NM_000022.4:c.479-47T>C MANE Select	NP_000013.2:n.479-47T>C
NM_001322050.2:c.74-47T>C	NP_001308979.1:n.74-47T>C
NM_001322051.2:c.479-47T>C	NP_001308980.1:n.479-47T>C
NR_136160.2:n.571-47T>C