Canonical Allele Identifier: CA2365869182
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651950G= , CM000682.2:g.44651950G= GRCh38
NC_000020.10:g.43280591G= , CM000682.1:g.43280591G= GRCh37
NC_000020.9:g.42714005G= NCBI36
NG_007385.1:g.4786C= , LRG_16:g.4786C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-169C= ENSP00000512234.1:n.-169C=
ENST00000696039.1:n.273C=
ENST00000696062.1:c.96+150C= ENSP00000512365.1:n.96+150C=
ENST00000696064.1:c.-166C= ENSP00000512367.1:n.-166C=
ENST00000535573.1:n.284C=
ENST00000536076.1:n.165C=
XM_011528479.1:c.-305C= XP_011526781.1:n.-305C=