Canonical Allele Identifier: CA510595331

Gene: ADA

Linked Data

• MyVariant Identifiers: chr20:g.43264909T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44636268T>C , CM000682.2:g.44636268T>C	GRCh38
NC_000020.10:g.43264909T>C , CM000682.1:g.43264909T>C	GRCh37
NC_000020.9:g.42698323T>C	NCBI36
NG_007385.1:g.20468A>G , LRG_16:g.20468A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000492931.6:n.145A>G
ENST00000536076.2:c.-100A>G	ENSP00000512234.1:n.-100A>G
ENST00000536532.6:c.54A>G	ENSP00000440946.1:p.Leu18=
ENST00000537820.2:c.54A>G	ENSP00000441818.1:p.Leu18=
ENST00000539235.6:c.54A>G	ENSP00000446464.1:p.Leu18=
ENST00000695889.1:c.54A>G	ENSP00000512240.1:p.Leu18=
ENST00000695891.1:c.54A>G	ENSP00000512241.1:p.Leu18=
ENST00000695927.1:c.132A>G	ENSP00000512270.1:p.Leu44=
ENST00000695949.1:c.54A>G	ENSP00000512281.1:p.Leu18=
ENST00000695957.1:c.54A>G	ENSP00000512286.1:p.Leu18=
ENST00000695991.1:c.54A>G	ENSP00000512314.1:p.Leu18=
ENST00000695992.1:c.54A>G	ENSP00000512315.1:p.Leu18=
ENST00000695993.1:c.54A>G	ENSP00000512316.1:p.Leu18=
ENST00000695994.1:c.54A>G	ENSP00000512317.1:p.Leu18=
ENST00000695995.1:c.54A>G	ENSP00000512318.1:p.Leu18=
ENST00000695996.1:n.125A>G
ENST00000695997.1:n.125A>G
ENST00000696003.1:n.146A>G
ENST00000696004.1:n.146A>G
ENST00000696006.1:c.54A>G	ENSP00000512325.1:p.Leu18=
ENST00000696007.1:c.21A>G	ENSP00000512326.1:p.Leu7=
ENST00000696009.1:n.165A>G
ENST00000696010.1:n.167A>G
ENST00000696017.1:c.54A>G	ENSP00000512333.1:p.Leu18=
ENST00000696034.1:c.54A>G	ENSP00000512343.1:p.Leu18=
ENST00000696038.1:c.54A>G	ENSP00000512344.1:p.Leu18=
ENST00000696039.1:n.342A>G
ENST00000696058.1:c.54A>G	ENSP00000512361.1:p.Leu18=
ENST00000696059.1:c.161A>G	ENSP00000512362.1:p.Ter54Trp
ENST00000696060.1:c.54A>G	ENSP00000512363.1:p.Leu18=
ENST00000696061.1:c.54A>G	ENSP00000512364.1:p.Leu18=
ENST00000696062.1:c.117A>G	ENSP00000512365.1:p.Leu39=
ENST00000696063.1:c.129A>G	ENSP00000512366.1:p.Leu43=
ENST00000696064.1:c.-97A>G	ENSP00000512367.1:n.-97A>G
ENST00000696065.1:c.-100A>G	ENSP00000512368.1:n.-100A>G
ENST00000696075.1:c.54A>G	ENSP00000512374.1:p.Leu18=
ENST00000696076.1:c.54A>G	ENSP00000512375.1:p.Leu18=
ENST00000696077.1:c.54A>G	ENSP00000512376.1:p.Leu18=
ENST00000696078.1:c.54A>G	ENSP00000512377.1:p.Leu18=
ENST00000696079.1:c.54A>G	ENSP00000512378.1:p.Leu18=
ENST00000696080.1:c.54A>G	ENSP00000512379.1:p.Leu18=
ENST00000696082.1:c.132A>G	ENSP00000512380.1:p.Leu44=
ENST00000696084.1:n.155A>G
ENST00000696104.1:c.54A>G	ENSP00000512399.1:p.Leu18=
ENST00000696105.1:c.54A>G	ENSP00000512400.1:p.Leu18=
ENST00000372874.9:c.54A>G MANE Select	ENSP00000361965.4:p.Leu18=
ENST00000372874.8:c.54A>G	ENSP00000361965.4:p.Leu18=
ENST00000492931.5:n.138A>G
ENST00000535573.1:n.353A>G
ENST00000536076.1:n.234A>G
ENST00000536532.5:c.54A>G	ENSP00000440946.1:p.Leu18=
ENST00000537820.1:c.54A>G	ENSP00000441818.1:p.Leu18=
ENST00000539235.5:c.54A>G	ENSP00000446464.1:p.Leu18=
ENST00000545776.5:n.108A>G
NM_000022.2:c.54A>G , LRG_16t1:c.54A>G	NP_000013.2:p.Leu18=
XM_005260236.2:c.54A>G	XP_005260293.1:p.Leu18=
XM_011528478.1:c.-236A>G	XP_011526780.1:n.-236A>G
XM_011528479.1:c.-236A>G	XP_011526781.1:n.-236A>G
XR_244129.1:n.108A>G
NM_000022.3:c.54A>G	NP_000013.2:p.Leu18=
NM_001322050.1:c.-236A>G	NP_001308979.1:n.-236A>G
NM_001322051.1:c.54A>G	NP_001308980.1:p.Leu18=
NR_136160.1:n.205A>G
NM_000022.4:c.54A>G MANE Select	NP_000013.2:p.Leu18=
NM_001322050.2:c.-236A>G	NP_001308979.1:n.-236A>G
NM_001322051.2:c.54A>G	NP_001308980.1:p.Leu18=
NR_136160.2:n.146A>G