Canonical Allele Identifier: CA2365869107
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651834A= , CM000682.2:g.44651834A= GRCh38
NC_000020.10:g.43280475A= , CM000682.1:g.43280475A= GRCh37
NC_000020.9:g.42713889A= NCBI36
NG_007385.1:g.4902T= , LRG_16:g.4902T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+68T= ENSP00000512234.1:n.-121+68T=
ENST00000696039.1:n.321+68T=
ENST00000696062.1:c.96+266T= ENSP00000512365.1:n.96+266T=
ENST00000696064.1:c.-118+68T= ENSP00000512367.1:n.-118+68T=
ENST00000696065.1:c.-121+68T= ENSP00000512368.1:n.-121+68T=
ENST00000535573.1:n.332+68T=
ENST00000536076.1:n.213+68T=
XM_011528479.1:c.-257+68T= XP_011526781.1:n.-257+68T=