Canonical Allele Identifier: CA2365869176
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651944C= , CM000682.2:g.44651944C= GRCh38
NC_000020.10:g.43280585C= , CM000682.1:g.43280585C= GRCh37
NC_000020.9:g.42713999C= NCBI36
NG_007385.1:g.4792G= , LRG_16:g.4792G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-163G= ENSP00000512234.1:n.-163G=
ENST00000696039.1:n.279G=
ENST00000696062.1:c.96+156G= ENSP00000512365.1:n.96+156G=
ENST00000696064.1:c.-160G= ENSP00000512367.1:n.-160G=
ENST00000535573.1:n.290G=
ENST00000536076.1:n.171G=
XM_011528479.1:c.-299G= XP_011526781.1:n.-299G=