Canonical Allele Identifier: CA2652991408

Gene: ADA

Linked Data

• gnomAD v4: 20-44626430-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44626430T>C , CM000682.2:g.44626430T>C	GRCh38
NC_000020.10:g.43255071T>C , CM000682.1:g.43255071T>C	GRCh37
NC_000020.9:g.42688485T>C	NCBI36
NG_007385.1:g.30306A>G , LRG_16:g.30306A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.453+26A>G
ENST00000536076.2:c.209+26A>G	ENSP00000512234.1:n.209+26A>G
ENST00000536532.6:c.362+26A>G	ENSP00000440946.1:n.362+26A>G
ENST00000537820.2:c.362+26A>G	ENSP00000441818.1:n.362+26A>G
ENST00000539235.6:c.218+2617A>G	ENSP00000446464.1:n.218+2617A>G
ENST00000695889.1:c.218+2617A>G	ENSP00000512240.1:n.218+2617A>G
ENST00000695890.1:n.2165+26A>G
ENST00000695891.1:c.218+2617A>G	ENSP00000512241.1:n.218+2617A>G
ENST00000695927.1:c.440+26A>G	ENSP00000512270.1:n.440+26A>G
ENST00000695949.1:c.359+26A>G	ENSP00000512281.1:n.359+26A>G
ENST00000695957.1:c.362+26A>G	ENSP00000512286.1:n.362+26A>G
ENST00000695991.1:c.216+2619A>G	ENSP00000512314.1:n.216+2619A>G
ENST00000695992.1:c.362+26A>G	ENSP00000512315.1:n.362+26A>G
ENST00000695993.1:c.362+26A>G	ENSP00000512316.1:n.362+26A>G
ENST00000695994.1:c.362+26A>G	ENSP00000512317.1:n.362+26A>G
ENST00000695995.1:c.216+2619A>G	ENSP00000512318.1:n.216+2619A>G
ENST00000695996.1:n.433+26A>G
ENST00000695997.1:n.433+26A>G
ENST00000696003.1:n.454+26A>G
ENST00000696004.1:n.454+26A>G
ENST00000696006.1:c.362+26A>G	ENSP00000512325.1:n.362+26A>G
ENST00000696007.1:c.329+26A>G	ENSP00000512326.1:n.329+26A>G
ENST00000696009.1:n.473+26A>G
ENST00000696017.1:c.359+26A>G	ENSP00000512333.1:n.359+26A>G
ENST00000696034.1:c.362+26A>G	ENSP00000512343.1:n.362+26A>G
ENST00000696035.1:n.472+26A>G
ENST00000696036.1:n.1052+26A>G
ENST00000696037.1:n.2039+26A>G
ENST00000696038.1:c.*108+26A>G	ENSP00000512344.1:n.*108+26A>G
ENST00000696039.1:n.650+26A>G
ENST00000696058.1:c.362+26A>G	ENSP00000512361.1:n.362+26A>G
ENST00000696059.1:c.*307+26A>G	ENSP00000512362.1:n.*307+26A>G
ENST00000696060.1:c.362+26A>G	ENSP00000512363.1:n.362+26A>G
ENST00000696061.1:c.359+26A>G	ENSP00000512364.1:n.359+26A>G
ENST00000696062.1:c.425+26A>G	ENSP00000512365.1:n.425+26A>G
ENST00000696063.1:c.437+26A>G	ENSP00000512366.1:n.437+26A>G
ENST00000696064.1:c.209+26A>G	ENSP00000512367.1:n.209+26A>G
ENST00000696065.1:c.65+2617A>G	ENSP00000512368.1:n.65+2617A>G
ENST00000696075.1:c.*332+26A>G	ENSP00000512374.1:n.*332+26A>G
ENST00000696076.1:c.362+26A>G	ENSP00000512375.1:n.362+26A>G
ENST00000696077.1:c.359+26A>G	ENSP00000512376.1:n.359+26A>G
ENST00000696078.1:c.362+26A>G	ENSP00000512377.1:n.362+26A>G
ENST00000696079.1:c.362+26A>G	ENSP00000512378.1:n.362+26A>G
ENST00000696080.1:c.362+26A>G	ENSP00000512379.1:n.362+26A>G
ENST00000696082.1:c.440+26A>G	ENSP00000512380.1:n.440+26A>G
ENST00000696084.1:n.463+26A>G
ENST00000696104.1:c.362+26A>G	ENSP00000512399.1:n.362+26A>G
ENST00000696105.1:c.362+26A>G	ENSP00000512400.1:n.362+26A>G
ENST00000372874.9:c.362+26A>G MANE Select	ENSP00000361965.4:n.362+26A>G
ENST00000372874.8:c.362+26A>G	ENSP00000361965.4:n.362+26A>G
ENST00000464097.5:n.36+26A>G
ENST00000492931.5:n.446+26A>G
ENST00000536532.5:c.362+26A>G	ENSP00000440946.1:n.362+26A>G
ENST00000537820.1:c.362+26A>G	ENSP00000441818.1:n.362+26A>G
ENST00000539235.5:c.218+2617A>G	ENSP00000446464.1:n.218+2617A>G
ENST00000545776.5:n.442A>G
NM_000022.2:c.362+26A>G , LRG_16t1:c.362+26A>G	NP_000013.2:n.362+26A>G
XM_005260236.2:c.362+26A>G	XP_005260293.1:n.362+26A>G
XM_011528478.1:c.73+26A>G	XP_011526780.1:n.73+26A>G
XM_011528479.1:c.73+26A>G	XP_011526781.1:n.73+26A>G
XR_244129.1:n.416+26A>G
NM_000022.3:c.362+26A>G	NP_000013.2:n.362+26A>G
NM_001322050.1:c.73+26A>G	NP_001308979.1:n.73+26A>G
NM_001322051.1:c.362+26A>G	NP_001308980.1:n.362+26A>G
NR_136160.1:n.513+26A>G
NM_000022.4:c.362+26A>G MANE Select	NP_000013.2:n.362+26A>G
NM_001322050.2:c.73+26A>G	NP_001308979.1:n.73+26A>G
NM_001322051.2:c.362+26A>G	NP_001308980.1:n.362+26A>G
NR_136160.2:n.454+26A>G