Canonical Allele Identifier: CA409122429

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43264871C>T (hg19) ; chr20:g.44636230C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44636230C>T , CM000682.2:g.44636230C>T	GRCh38
NC_000020.10:g.43264871C>T , CM000682.1:g.43264871C>T	GRCh37
NC_000020.9:g.42698285C>T	NCBI36
NG_007385.1:g.20506G>A , LRG_16:g.20506G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.183G>A
ENST00000536076.2:c.-62G>A	ENSP00000512234.1:n.-62G>A
ENST00000536532.6:c.92G>A	ENSP00000440946.1:p.Gly31Asp
ENST00000537820.2:c.92G>A	ENSP00000441818.1:p.Gly31Asp
ENST00000539235.6:c.92G>A	ENSP00000446464.1:p.Gly31Asp
ENST00000695889.1:c.92G>A	ENSP00000512240.1:p.Gly31Asp
ENST00000695891.1:c.92G>A	ENSP00000512241.1:p.Gly31Asp
ENST00000695927.1:c.170G>A	ENSP00000512270.1:p.Gly57Asp
ENST00000695949.1:c.92G>A	ENSP00000512281.1:p.Gly31Asp
ENST00000695957.1:c.92G>A	ENSP00000512286.1:p.Gly31Asp
ENST00000695991.1:c.92G>A	ENSP00000512314.1:p.Gly31Asp
ENST00000695992.1:c.92G>A	ENSP00000512315.1:p.Gly31Asp
ENST00000695993.1:c.92G>A	ENSP00000512316.1:p.Gly31Asp
ENST00000695994.1:c.92G>A	ENSP00000512317.1:p.Gly31Asp
ENST00000695995.1:c.92G>A	ENSP00000512318.1:p.Gly31Asp
ENST00000695996.1:n.163G>A
ENST00000695997.1:n.163G>A
ENST00000696003.1:n.184G>A
ENST00000696004.1:n.184G>A
ENST00000696006.1:c.92G>A	ENSP00000512325.1:p.Gly31Asp
ENST00000696007.1:c.59G>A	ENSP00000512326.1:p.Gly20Asp
ENST00000696009.1:n.203G>A
ENST00000696010.1:n.205G>A
ENST00000696017.1:c.92G>A	ENSP00000512333.1:p.Gly31Asp
ENST00000696034.1:c.92G>A	ENSP00000512343.1:p.Gly31Asp
ENST00000696038.1:c.92G>A	ENSP00000512344.1:p.Gly31Asp
ENST00000696039.1:n.380G>A
ENST00000696058.1:c.92G>A	ENSP00000512361.1:p.Gly31Asp
ENST00000696059.1:c.*37G>A	ENSP00000512362.1:n.*37G>A
ENST00000696060.1:c.92G>A	ENSP00000512363.1:p.Gly31Asp
ENST00000696061.1:c.92G>A	ENSP00000512364.1:p.Gly31Asp
ENST00000696062.1:c.155G>A	ENSP00000512365.1:p.Gly52Asp
ENST00000696063.1:c.167G>A	ENSP00000512366.1:p.Gly56Asp
ENST00000696064.1:c.-59G>A	ENSP00000512367.1:n.-59G>A
ENST00000696065.1:c.-62G>A	ENSP00000512368.1:n.-62G>A
ENST00000696075.1:c.92G>A	ENSP00000512374.1:p.Gly31Asp
ENST00000696076.1:c.92G>A	ENSP00000512375.1:p.Gly31Asp
ENST00000696077.1:c.92G>A	ENSP00000512376.1:p.Gly31Asp
ENST00000696078.1:c.92G>A	ENSP00000512377.1:p.Gly31Asp
ENST00000696079.1:c.92G>A	ENSP00000512378.1:p.Gly31Asp
ENST00000696080.1:c.92G>A	ENSP00000512379.1:p.Gly31Asp
ENST00000696082.1:c.170G>A	ENSP00000512380.1:p.Gly57Asp
ENST00000696084.1:n.193G>A
ENST00000696104.1:c.92G>A	ENSP00000512399.1:p.Gly31Asp
ENST00000696105.1:c.92G>A	ENSP00000512400.1:p.Gly31Asp
ENST00000372874.9:c.92G>A MANE Select	ENSP00000361965.4:p.Gly31Asp
ENST00000372874.8:c.92G>A	ENSP00000361965.4:p.Gly31Asp
ENST00000492931.5:n.176G>A
ENST00000535573.1:n.391G>A
ENST00000536076.1:n.272G>A
ENST00000536532.5:c.92G>A	ENSP00000440946.1:p.Gly31Asp
ENST00000537820.1:c.92G>A	ENSP00000441818.1:p.Gly31Asp
ENST00000539235.5:c.92G>A	ENSP00000446464.1:p.Gly31Asp
ENST00000545776.5:n.146G>A
NM_000022.2:c.92G>A , LRG_16t1:c.92G>A	NP_000013.2:p.Gly31Asp
XM_005260236.2:c.92G>A	XP_005260293.1:p.Gly31Asp
XM_011528478.1:c.-198G>A	XP_011526780.1:n.-198G>A
XM_011528479.1:c.-198G>A	XP_011526781.1:n.-198G>A
XR_244129.1:n.146G>A
NM_000022.3:c.92G>A	NP_000013.2:p.Gly31Asp
NM_001322050.1:c.-198G>A	NP_001308979.1:n.-198G>A
NM_001322051.1:c.92G>A	NP_001308980.1:p.Gly31Asp
NR_136160.1:n.243G>A
NM_000022.4:c.92G>A MANE Select	NP_000013.2:p.Gly31Asp
NM_001322050.2:c.-198G>A	NP_001308979.1:n.-198G>A
NM_001322051.2:c.92G>A	NP_001308980.1:p.Gly31Asp
NR_136160.2:n.184G>A