Canonical Allele Identifier: CA2365868999
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651709G= , CM000682.2:g.44651709G= GRCh38
NC_000020.10:g.43280350G= , CM000682.1:g.43280350G= GRCh37
NC_000020.9:g.42713764G= NCBI36
NG_007385.1:g.5027C= , LRG_16:g.5027C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+193C= ENSP00000512234.1:n.-121+193C=
ENST00000537820.2:c.-102C= ENSP00000441818.1:n.-102C=
ENST00000695949.1:c.-102C= ENSP00000512281.1:n.-102C=
ENST00000695993.1:c.-102C= ENSP00000512316.1:n.-102C=
ENST00000696006.1:c.-102C= ENSP00000512325.1:n.-102C=
ENST00000696009.1:n.10C=
ENST00000696010.1:n.12C=
ENST00000696039.1:n.321+193C=
ENST00000696059.1:c.-102C= ENSP00000512362.1:n.-102C=
ENST00000696060.1:c.-102C= ENSP00000512363.1:n.-102C=
ENST00000696061.1:c.-102C= ENSP00000512364.1:n.-102C=
ENST00000696062.1:c.96+391C= ENSP00000512365.1:n.96+391C=
ENST00000696064.1:c.-118+193C= ENSP00000512367.1:n.-118+193C=
ENST00000696065.1:c.-121+193C= ENSP00000512368.1:n.-121+193C=
ENST00000696076.1:c.-102C= ENSP00000512375.1:n.-102C=
ENST00000696077.1:c.-102C= ENSP00000512376.1:n.-102C=
ENST00000696078.1:c.-102C= ENSP00000512377.1:n.-102C=
ENST00000696080.1:c.-102C= ENSP00000512379.1:n.-102C=
ENST00000372874.8:c.-102C= ENSP00000361965.4:n.-102C=
ENST00000535573.1:n.332+193C=
ENST00000536076.1:n.213+193C=
NM_000022.2:c.-102C= , LRG_16t1:c.-102C= NP_000013.2:n.-102C=
XM_011528479.1:c.-257+193C= XP_011526781.1:n.-257+193C=
NM_000022.3:c.-102C= NP_000013.2:n.-102C=
NM_001322050.1:c.-391C= NP_001308979.1:n.-391C=
NM_001322051.1:c.-102C= NP_001308980.1:n.-102C=
NR_136160.1:n.50C=