Canonical Allele Identifier: CA2365869160
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651925C= , CM000682.2:g.44651925C= GRCh38
NC_000020.10:g.43280566C= , CM000682.1:g.43280566C= GRCh37
NC_000020.9:g.42713980C= NCBI36
NG_007385.1:g.4811G= , LRG_16:g.4811G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-144G= ENSP00000512234.1:n.-144G=
ENST00000696039.1:n.298G=
ENST00000696062.1:c.96+175G= ENSP00000512365.1:n.96+175G=
ENST00000696064.1:c.-141G= ENSP00000512367.1:n.-141G=
ENST00000535573.1:n.309G=
ENST00000536076.1:n.190G=
XM_011528479.1:c.-280G= XP_011526781.1:n.-280G=