Canonical Allele Identifier: CA2365869163
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651927C= , CM000682.2:g.44651927C= GRCh38
NC_000020.10:g.43280568C= , CM000682.1:g.43280568C= GRCh37
NC_000020.9:g.42713982C= NCBI36
NG_007385.1:g.4809G= , LRG_16:g.4809G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-146G= ENSP00000512234.1:n.-146G=
ENST00000696039.1:n.296G=
ENST00000696062.1:c.96+173G= ENSP00000512365.1:n.96+173G=
ENST00000696064.1:c.-143G= ENSP00000512367.1:n.-143G=
ENST00000535573.1:n.307G=
ENST00000536076.1:n.188G=
XM_011528479.1:c.-282G= XP_011526781.1:n.-282G=