Canonical Allele Identifier: CA2365869157
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651918C= , CM000682.2:g.44651918C= GRCh38
NC_000020.10:g.43280559C= , CM000682.1:g.43280559C= GRCh37
NC_000020.9:g.42713973C= NCBI36
NG_007385.1:g.4818G= , LRG_16:g.4818G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-137G= ENSP00000512234.1:n.-137G=
ENST00000696039.1:n.305G=
ENST00000696062.1:c.96+182G= ENSP00000512365.1:n.96+182G=
ENST00000696064.1:c.-134G= ENSP00000512367.1:n.-134G=
ENST00000535573.1:n.316G=
ENST00000536076.1:n.197G=
XM_011528479.1:c.-273G= XP_011526781.1:n.-273G=