Canonical Allele Identifier: CA409121395

Gene: ADA

Linked Data

• dbSNP Id: rs1437613842
• gnomAD v2: 20-43255162-C-G
• gnomAD v4: 20-44626521-C-G
• MyVariant Identifiers: chr20:g.43255162C>G (hg19) ; chr20:g.44626521C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44626521C>G , CM000682.2:g.44626521C>G	GRCh38
NC_000020.10:g.43255162C>G , CM000682.1:g.43255162C>G	GRCh37
NC_000020.9:g.42688576C>G	NCBI36
NG_007385.1:g.30215G>C , LRG_16:g.30215G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.388G>C
ENST00000536076.2:c.144G>C	ENSP00000512234.1:p.Glu48Asp
ENST00000536532.6:c.297G>C	ENSP00000440946.1:p.Glu99Asp
ENST00000537820.2:c.297G>C	ENSP00000441818.1:p.Glu99Asp
ENST00000539235.6:c.218+2526G>C	ENSP00000446464.1:n.218+2526G>C
ENST00000695889.1:c.218+2526G>C	ENSP00000512240.1:n.218+2526G>C
ENST00000695890.1:n.2100G>C
ENST00000695891.1:c.218+2526G>C	ENSP00000512241.1:n.218+2526G>C
ENST00000695927.1:c.375G>C	ENSP00000512270.1:p.Glu125Asp
ENST00000695949.1:c.294G>C	ENSP00000512281.1:p.Glu98Asp
ENST00000695957.1:c.297G>C	ENSP00000512286.1:p.Glu99Asp
ENST00000695991.1:c.216+2528G>C	ENSP00000512314.1:n.216+2528G>C
ENST00000695992.1:c.297G>C	ENSP00000512315.1:p.Glu99Asp
ENST00000695993.1:c.297G>C	ENSP00000512316.1:p.Glu99Asp
ENST00000695994.1:c.297G>C	ENSP00000512317.1:p.Glu99Asp
ENST00000695995.1:c.216+2528G>C	ENSP00000512318.1:n.216+2528G>C
ENST00000695996.1:n.368G>C
ENST00000695997.1:n.368G>C
ENST00000696003.1:n.389G>C
ENST00000696004.1:n.389G>C
ENST00000696006.1:c.297G>C	ENSP00000512325.1:p.Glu99Asp
ENST00000696007.1:c.264G>C	ENSP00000512326.1:p.Glu88Asp
ENST00000696009.1:n.408G>C
ENST00000696017.1:c.294G>C	ENSP00000512333.1:p.Glu98Asp
ENST00000696034.1:c.297G>C	ENSP00000512343.1:p.Glu99Asp
ENST00000696035.1:n.407G>C
ENST00000696036.1:n.987G>C
ENST00000696037.1:n.1974G>C
ENST00000696038.1:c.*43G>C	ENSP00000512344.1:n.*43G>C
ENST00000696039.1:n.585G>C
ENST00000696058.1:c.297G>C	ENSP00000512361.1:p.Glu99Asp
ENST00000696059.1:c.*242G>C	ENSP00000512362.1:n.*242G>C
ENST00000696060.1:c.297G>C	ENSP00000512363.1:p.Glu99Asp
ENST00000696061.1:c.294G>C	ENSP00000512364.1:p.Glu98Asp
ENST00000696062.1:c.360G>C	ENSP00000512365.1:p.Glu120Asp
ENST00000696063.1:c.372G>C	ENSP00000512366.1:p.Glu124Asp
ENST00000696064.1:c.144G>C	ENSP00000512367.1:p.Glu48Asp
ENST00000696065.1:c.65+2526G>C	ENSP00000512368.1:n.65+2526G>C
ENST00000696075.1:c.*267G>C	ENSP00000512374.1:n.*267G>C
ENST00000696076.1:c.297G>C	ENSP00000512375.1:p.Glu99Asp
ENST00000696077.1:c.294G>C	ENSP00000512376.1:p.Glu98Asp
ENST00000696078.1:c.297G>C	ENSP00000512377.1:p.Glu99Asp
ENST00000696079.1:c.297G>C	ENSP00000512378.1:p.Glu99Asp
ENST00000696080.1:c.297G>C	ENSP00000512379.1:p.Glu99Asp
ENST00000696082.1:c.375G>C	ENSP00000512380.1:p.Glu125Asp
ENST00000696084.1:n.398G>C
ENST00000696104.1:c.297G>C	ENSP00000512399.1:p.Glu99Asp
ENST00000696105.1:c.297G>C	ENSP00000512400.1:p.Glu99Asp
ENST00000372874.9:c.297G>C MANE Select	ENSP00000361965.4:p.Glu99Asp
ENST00000372874.8:c.297G>C	ENSP00000361965.4:p.Glu99Asp
ENST00000492931.5:n.381G>C
ENST00000536076.1:n.477G>C
ENST00000536532.5:c.297G>C	ENSP00000440946.1:p.Glu99Asp
ENST00000537820.1:c.297G>C	ENSP00000441818.1:p.Glu99Asp
ENST00000539235.5:c.218+2526G>C	ENSP00000446464.1:n.218+2526G>C
ENST00000545776.5:n.351G>C
NM_000022.2:c.297G>C , LRG_16t1:c.297G>C	NP_000013.2:p.Glu99Asp
XM_005260236.2:c.297G>C	XP_005260293.1:p.Glu99Asp
XM_011528478.1:c.8G>C	XP_011526780.1:p.Arg3Thr
XM_011528479.1:c.8G>C	XP_011526781.1:p.Arg3Thr
XR_244129.1:n.351G>C
NM_000022.3:c.297G>C	NP_000013.2:p.Glu99Asp
NM_001322050.1:c.8G>C	NP_001308979.1:p.Arg3Thr
NM_001322051.1:c.297G>C	NP_001308980.1:p.Glu99Asp
NR_136160.1:n.448G>C
NM_000022.4:c.297G>C MANE Select	NP_000013.2:p.Glu99Asp
NM_001322050.2:c.8G>C	NP_001308979.1:p.Arg3Thr
NM_001322051.2:c.297G>C	NP_001308980.1:p.Glu99Asp
NR_136160.2:n.389G>C