Canonical Allele Identifier: CA409122494

Gene: ADA

Linked Data

• gnomAD v4: 20-44636263-C-A
• MyVariant Identifiers: chr20:g.43264904C>A (hg19) ; chr20:g.44636263C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44636263C>A , CM000682.2:g.44636263C>A	GRCh38
NC_000020.10:g.43264904C>A , CM000682.1:g.43264904C>A	GRCh37
NC_000020.9:g.42698318C>A	NCBI36
NG_007385.1:g.20473G>T , LRG_16:g.20473G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492931.6:n.150G>T
ENST00000536076.2:c.-95G>T	ENSP00000512234.1:n.-95G>T
ENST00000536532.6:c.59G>T	ENSP00000440946.1:p.Gly20Val
ENST00000537820.2:c.59G>T	ENSP00000441818.1:p.Gly20Val
ENST00000539235.6:c.59G>T	ENSP00000446464.1:p.Gly20Val
ENST00000695889.1:c.59G>T	ENSP00000512240.1:p.Gly20Val
ENST00000695891.1:c.59G>T	ENSP00000512241.1:p.Gly20Val
ENST00000695927.1:c.137G>T	ENSP00000512270.1:p.Gly46Val
ENST00000695949.1:c.59G>T	ENSP00000512281.1:p.Gly20Val
ENST00000695957.1:c.59G>T	ENSP00000512286.1:p.Gly20Val
ENST00000695991.1:c.59G>T	ENSP00000512314.1:p.Gly20Val
ENST00000695992.1:c.59G>T	ENSP00000512315.1:p.Gly20Val
ENST00000695993.1:c.59G>T	ENSP00000512316.1:p.Gly20Val
ENST00000695994.1:c.59G>T	ENSP00000512317.1:p.Gly20Val
ENST00000695995.1:c.59G>T	ENSP00000512318.1:p.Gly20Val
ENST00000695996.1:n.130G>T
ENST00000695997.1:n.130G>T
ENST00000696003.1:n.151G>T
ENST00000696004.1:n.151G>T
ENST00000696006.1:c.59G>T	ENSP00000512325.1:p.Gly20Val
ENST00000696007.1:c.26G>T	ENSP00000512326.1:p.Gly9Val
ENST00000696009.1:n.170G>T
ENST00000696010.1:n.172G>T
ENST00000696017.1:c.59G>T	ENSP00000512333.1:p.Gly20Val
ENST00000696034.1:c.59G>T	ENSP00000512343.1:p.Gly20Val
ENST00000696038.1:c.59G>T	ENSP00000512344.1:p.Gly20Val
ENST00000696039.1:n.347G>T
ENST00000696058.1:c.59G>T	ENSP00000512361.1:p.Gly20Val
ENST00000696059.1:c.*4G>T	ENSP00000512362.1:n.*4G>T
ENST00000696060.1:c.59G>T	ENSP00000512363.1:p.Gly20Val
ENST00000696061.1:c.59G>T	ENSP00000512364.1:p.Gly20Val
ENST00000696062.1:c.122G>T	ENSP00000512365.1:p.Gly41Val
ENST00000696063.1:c.134G>T	ENSP00000512366.1:p.Gly45Val
ENST00000696064.1:c.-92G>T	ENSP00000512367.1:n.-92G>T
ENST00000696065.1:c.-95G>T	ENSP00000512368.1:n.-95G>T
ENST00000696075.1:c.59G>T	ENSP00000512374.1:p.Gly20Val
ENST00000696076.1:c.59G>T	ENSP00000512375.1:p.Gly20Val
ENST00000696077.1:c.59G>T	ENSP00000512376.1:p.Gly20Val
ENST00000696078.1:c.59G>T	ENSP00000512377.1:p.Gly20Val
ENST00000696079.1:c.59G>T	ENSP00000512378.1:p.Gly20Val
ENST00000696080.1:c.59G>T	ENSP00000512379.1:p.Gly20Val
ENST00000696082.1:c.137G>T	ENSP00000512380.1:p.Gly46Val
ENST00000696084.1:n.160G>T
ENST00000696104.1:c.59G>T	ENSP00000512399.1:p.Gly20Val
ENST00000696105.1:c.59G>T	ENSP00000512400.1:p.Gly20Val
ENST00000372874.9:c.59G>T MANE Select	ENSP00000361965.4:p.Gly20Val
ENST00000372874.8:c.59G>T	ENSP00000361965.4:p.Gly20Val
ENST00000492931.5:n.143G>T
ENST00000535573.1:n.358G>T
ENST00000536076.1:n.239G>T
ENST00000536532.5:c.59G>T	ENSP00000440946.1:p.Gly20Val
ENST00000537820.1:c.59G>T	ENSP00000441818.1:p.Gly20Val
ENST00000539235.5:c.59G>T	ENSP00000446464.1:p.Gly20Val
ENST00000545776.5:n.113G>T
NM_000022.2:c.59G>T , LRG_16t1:c.59G>T	NP_000013.2:p.Gly20Val
XM_005260236.2:c.59G>T	XP_005260293.1:p.Gly20Val
XM_011528478.1:c.-231G>T	XP_011526780.1:n.-231G>T
XM_011528479.1:c.-231G>T	XP_011526781.1:n.-231G>T
XR_244129.1:n.113G>T
NM_000022.3:c.59G>T	NP_000013.2:p.Gly20Val
NM_001322050.1:c.-231G>T	NP_001308979.1:n.-231G>T
NM_001322051.1:c.59G>T	NP_001308980.1:p.Gly20Val
NR_136160.1:n.210G>T
NM_000022.4:c.59G>T MANE Select	NP_000013.2:p.Gly20Val
NM_001322050.2:c.-231G>T	NP_001308979.1:n.-231G>T
NM_001322051.2:c.59G>T	NP_001308980.1:p.Gly20Val
NR_136160.2:n.151G>T