Canonical Allele Identifier: CA2365869175
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651943C= , CM000682.2:g.44651943C= GRCh38
NC_000020.10:g.43280584C= , CM000682.1:g.43280584C= GRCh37
NC_000020.9:g.42713998C= NCBI36
NG_007385.1:g.4793G= , LRG_16:g.4793G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-162G= ENSP00000512234.1:n.-162G=
ENST00000696039.1:n.280G=
ENST00000696062.1:c.96+157G= ENSP00000512365.1:n.96+157G=
ENST00000696064.1:c.-159G= ENSP00000512367.1:n.-159G=
ENST00000535573.1:n.291G=
ENST00000536076.1:n.172G=
XM_011528479.1:c.-298G= XP_011526781.1:n.-298G=