Canonical Allele Identifier: CA2365869179
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651947C= , CM000682.2:g.44651947C= GRCh38
NC_000020.10:g.43280588C= , CM000682.1:g.43280588C= GRCh37
NC_000020.9:g.42714002C= NCBI36
NG_007385.1:g.4789G= , LRG_16:g.4789G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-166G= ENSP00000512234.1:n.-166G=
ENST00000696039.1:n.276G=
ENST00000696062.1:c.96+153G= ENSP00000512365.1:n.96+153G=
ENST00000696064.1:c.-163G= ENSP00000512367.1:n.-163G=
ENST00000535573.1:n.287G=
ENST00000536076.1:n.168G=
XM_011528479.1:c.-302G= XP_011526781.1:n.-302G=