Canonical Allele Identifier: CA2365869158
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651922C= , CM000682.2:g.44651922C= GRCh38
NC_000020.10:g.43280563C= , CM000682.1:g.43280563C= GRCh37
NC_000020.9:g.42713977C= NCBI36
NG_007385.1:g.4814G= , LRG_16:g.4814G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-141G= ENSP00000512234.1:n.-141G=
ENST00000696039.1:n.301G=
ENST00000696062.1:c.96+178G= ENSP00000512365.1:n.96+178G=
ENST00000696064.1:c.-138G= ENSP00000512367.1:n.-138G=
ENST00000535573.1:n.312G=
ENST00000536076.1:n.193G=
XM_011528479.1:c.-277G= XP_011526781.1:n.-277G=