Canonical Allele Identifier: CA409121079

Gene: ADA

Linked Data

• gnomAD v4: 20-44625598-G-T
• MyVariant Identifiers: chr20:g.43254239G>T (hg19) ; chr20:g.44625598G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44625598G>T , CM000682.2:g.44625598G>T	GRCh38
NC_000020.10:g.43254239G>T , CM000682.1:g.43254239G>T	GRCh37
NC_000020.9:g.42687653G>T	NCBI36
NG_007385.1:g.31138C>A , LRG_16:g.31138C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.540C>A
ENST00000536076.2:c.296C>A	ENSP00000512234.1:p.Ser99Tyr
ENST00000536532.6:c.449C>A	ENSP00000440946.1:p.Ser150Tyr
ENST00000537820.2:c.449C>A	ENSP00000441818.1:p.Ser150Tyr
ENST00000539235.6:c.219-2520C>A	ENSP00000446464.1:n.219-2520C>A
ENST00000695889.1:c.219-2668C>A	ENSP00000512240.1:n.219-2668C>A
ENST00000695890.1:n.2252C>A
ENST00000695891.1:c.219-2668C>A	ENSP00000512241.1:n.219-2668C>A
ENST00000695927.1:c.527C>A	ENSP00000512270.1:p.Ser176Tyr
ENST00000695949.1:c.446C>A	ENSP00000512281.1:p.Ser149Tyr
ENST00000695957.1:c.362+858C>A	ENSP00000512286.1:n.362+858C>A
ENST00000695991.1:c.217-2668C>A	ENSP00000512314.1:n.217-2668C>A
ENST00000695992.1:c.449C>A	ENSP00000512315.1:p.Ser150Tyr
ENST00000695993.1:c.449C>A	ENSP00000512316.1:p.Ser150Tyr
ENST00000695994.1:c.449C>A	ENSP00000512317.1:p.Ser150Tyr
ENST00000695995.1:c.217-2520C>A	ENSP00000512318.1:n.217-2520C>A
ENST00000695996.1:n.520C>A
ENST00000695997.1:n.433+858C>A
ENST00000696003.1:n.541C>A
ENST00000696004.1:n.541C>A
ENST00000696006.1:c.449C>A	ENSP00000512325.1:p.Ser150Tyr
ENST00000696007.1:c.329+858C>A	ENSP00000512326.1:n.329+858C>A
ENST00000696008.1:n.365C>A
ENST00000696009.1:n.560C>A
ENST00000696017.1:c.446C>A	ENSP00000512333.1:p.Ser149Tyr
ENST00000696034.1:c.449C>A	ENSP00000512343.1:p.Ser150Tyr
ENST00000696035.1:n.559C>A
ENST00000696036.1:n.1139C>A
ENST00000696037.1:n.2126C>A
ENST00000696038.1:c.*195C>A	ENSP00000512344.1:n.*195C>A
ENST00000696039.1:n.737C>A
ENST00000696058.1:c.449C>A	ENSP00000512361.1:p.Ser150Tyr
ENST00000696059.1:c.*394C>A	ENSP00000512362.1:n.*394C>A
ENST00000696060.1:c.449C>A	ENSP00000512363.1:p.Ser150Tyr
ENST00000696061.1:c.446C>A	ENSP00000512364.1:p.Ser149Tyr
ENST00000696062.1:c.512C>A	ENSP00000512365.1:p.Ser171Tyr
ENST00000696063.1:c.524C>A	ENSP00000512366.1:p.Ser175Tyr
ENST00000696064.1:c.296C>A	ENSP00000512367.1:p.Ser99Tyr
ENST00000696065.1:c.66-2668C>A	ENSP00000512368.1:n.66-2668C>A
ENST00000696075.1:c.*419C>A	ENSP00000512374.1:n.*419C>A
ENST00000696076.1:c.449C>A	ENSP00000512375.1:p.Ser150Tyr
ENST00000696077.1:c.446C>A	ENSP00000512376.1:p.Ser149Tyr
ENST00000696078.1:c.449C>A	ENSP00000512377.1:p.Ser150Tyr
ENST00000696079.1:c.449C>A	ENSP00000512378.1:p.Ser150Tyr
ENST00000696080.1:c.449C>A	ENSP00000512379.1:p.Ser150Tyr
ENST00000696082.1:c.527C>A	ENSP00000512380.1:p.Ser176Tyr
ENST00000696083.1:n.91C>A
ENST00000696084.1:n.550C>A
ENST00000696104.1:c.362+858C>A	ENSP00000512399.1:n.362+858C>A
ENST00000696105.1:c.449C>A	ENSP00000512400.1:p.Ser150Tyr
ENST00000372874.9:c.449C>A MANE Select	ENSP00000361965.4:p.Ser150Tyr
ENST00000372874.8:c.449C>A	ENSP00000361965.4:p.Ser150Tyr
ENST00000464097.5:n.123C>A
ENST00000492931.5:n.533C>A
ENST00000536532.5:c.449C>A	ENSP00000440946.1:p.Ser150Tyr
ENST00000537820.1:c.449C>A	ENSP00000441818.1:p.Ser150Tyr
ENST00000539235.5:c.219-2520C>A	ENSP00000446464.1:n.219-2520C>A
NM_000022.2:c.449C>A , LRG_16t1:c.449C>A	NP_000013.2:p.Ser150Tyr
XM_005260236.2:c.449C>A	XP_005260293.1:p.Ser150Tyr
XM_011528478.1:c.73+858C>A	XP_011526780.1:n.73+858C>A
XM_011528479.1:c.73+858C>A	XP_011526781.1:n.73+858C>A
XR_244129.1:n.503C>A
NM_000022.3:c.449C>A	NP_000013.2:p.Ser150Tyr
NM_001322050.1:c.73+858C>A	NP_001308979.1:n.73+858C>A
NM_001322051.1:c.449C>A	NP_001308980.1:p.Ser150Tyr
NR_136160.1:n.600C>A
NM_000022.4:c.449C>A MANE Select	NP_000013.2:p.Ser150Tyr
NM_001322050.2:c.73+858C>A	NP_001308979.1:n.73+858C>A
NM_001322051.2:c.449C>A	NP_001308980.1:p.Ser150Tyr
NR_136160.2:n.541C>A