Canonical Allele Identifier: CA409120885

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43252916A>C (hg19) ; chr20:g.44624275A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44624275A>C , CM000682.2:g.44624275A>C	GRCh38
NC_000020.10:g.43252916A>C , CM000682.1:g.43252916A>C	GRCh37
NC_000020.9:g.42686330A>C	NCBI36
NG_007385.1:g.32461T>G , LRG_16:g.32461T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.624T>G
ENST00000536076.2:c.380T>G	ENSP00000512234.1:p.Val127Gly
ENST00000536532.6:c.533T>G	ENSP00000440946.1:p.Val178Gly
ENST00000537820.2:c.533T>G	ENSP00000441818.1:p.Val178Gly
ENST00000539235.6:c.219-1197T>G	ENSP00000446464.1:n.219-1197T>G
ENST00000695889.1:c.219-1345T>G	ENSP00000512240.1:n.219-1345T>G
ENST00000695890.1:n.2336T>G
ENST00000695891.1:c.219-1345T>G	ENSP00000512241.1:n.219-1345T>G
ENST00000695927.1:c.611T>G	ENSP00000512270.1:p.Val204Gly
ENST00000695949.1:c.530T>G	ENSP00000512281.1:p.Val177Gly
ENST00000695957.1:c.*24T>G	ENSP00000512286.1:n.*24T>G
ENST00000695991.1:c.217-1345T>G	ENSP00000512314.1:n.217-1345T>G
ENST00000695992.1:c.533T>G	ENSP00000512315.1:p.Val178Gly
ENST00000695993.1:c.533T>G	ENSP00000512316.1:p.Val178Gly
ENST00000695994.1:c.533T>G	ENSP00000512317.1:p.Val178Gly
ENST00000695995.1:c.217-1197T>G	ENSP00000512318.1:n.217-1197T>G
ENST00000695996.1:n.604T>G
ENST00000695997.1:n.488T>G
ENST00000696003.1:n.625T>G
ENST00000696004.1:n.625T>G
ENST00000696005.1:c.55T>G
ENST00000696006.1:c.533T>G	ENSP00000512325.1:p.Val178Gly
ENST00000696007.1:c.384T>G	ENSP00000512326.1:n.384T>G
ENST00000696008.1:n.1688T>G
ENST00000696009.1:n.1883T>G
ENST00000696017.1:c.530T>G	ENSP00000512333.1:p.Val177Gly
ENST00000696034.1:c.533T>G	ENSP00000512343.1:p.Val178Gly
ENST00000696035.1:n.643T>G
ENST00000696036.1:n.1223T>G
ENST00000696037.1:n.2210T>G
ENST00000696038.1:c.*279T>G	ENSP00000512344.1:n.*279T>G
ENST00000696039.1:n.821T>G
ENST00000696058.1:c.533T>G	ENSP00000512361.1:p.Val178Gly
ENST00000696059.1:c.*478T>G	ENSP00000512362.1:n.*478T>G
ENST00000696060.1:c.533T>G	ENSP00000512363.1:p.Val178Gly
ENST00000696061.1:c.530T>G	ENSP00000512364.1:p.Val177Gly
ENST00000696062.1:c.596T>G	ENSP00000512365.1:p.Val199Gly
ENST00000696063.1:c.608T>G	ENSP00000512366.1:p.Val203Gly
ENST00000696064.1:c.380T>G	ENSP00000512367.1:p.Val127Gly
ENST00000696065.1:c.66-1345T>G	ENSP00000512368.1:n.66-1345T>G
ENST00000696074.1:n.149T>G
ENST00000696075.1:c.*503T>G	ENSP00000512374.1:n.*503T>G
ENST00000696076.1:c.533T>G	ENSP00000512375.1:p.Val178Gly
ENST00000696077.1:c.530T>G	ENSP00000512376.1:p.Val177Gly
ENST00000696078.1:c.533T>G	ENSP00000512377.1:p.Val178Gly
ENST00000696079.1:c.533T>G	ENSP00000512378.1:p.Val178Gly
ENST00000696080.1:c.533T>G	ENSP00000512379.1:p.Val178Gly
ENST00000696081.1:n.652T>G
ENST00000696082.1:c.611T>G	ENSP00000512380.1:p.Val204Gly
ENST00000696083.1:n.1414T>G
ENST00000696084.1:n.634T>G
ENST00000696104.1:c.363-1345T>G	ENSP00000512399.1:n.363-1345T>G
ENST00000696105.1:c.*74T>G	ENSP00000512400.1:n.*74T>G
ENST00000372874.9:c.533T>G MANE Select	ENSP00000361965.4:p.Val178Gly
ENST00000372874.8:c.533T>G	ENSP00000361965.4:p.Val178Gly
ENST00000464097.5:n.207T>G
ENST00000492931.5:n.617T>G
ENST00000536532.5:c.533T>G	ENSP00000440946.1:p.Val178Gly
ENST00000537820.1:c.533T>G	ENSP00000441818.1:p.Val178Gly
ENST00000539235.5:c.219-1197T>G	ENSP00000446464.1:n.219-1197T>G
NM_000022.2:c.533T>G , LRG_16t1:c.533T>G	NP_000013.2:p.Val178Gly
XM_005260236.2:c.533T>G	XP_005260293.1:p.Val178Gly
XM_011528478.1:c.128T>G	XP_011526780.1:p.Val43Gly
XM_011528479.1:c.128T>G	XP_011526781.1:p.Val43Gly
XR_244129.1:n.587T>G
NM_000022.3:c.533T>G	NP_000013.2:p.Val178Gly
NM_001322050.1:c.128T>G	NP_001308979.1:p.Val43Gly
NM_001322051.1:c.533T>G	NP_001308980.1:p.Val178Gly
NR_136160.1:n.684T>G
NM_000022.4:c.533T>G MANE Select	NP_000013.2:p.Val178Gly
NM_001322050.2:c.128T>G	NP_001308979.1:p.Val43Gly
NM_001322051.2:c.533T>G	NP_001308980.1:p.Val178Gly
NR_136160.2:n.625T>G