Canonical Allele Identifier: CA2365869153
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651914G= , CM000682.2:g.44651914G= GRCh38
NC_000020.10:g.43280555G= , CM000682.1:g.43280555G= GRCh37
NC_000020.9:g.42713969G= NCBI36
NG_007385.1:g.4822C= , LRG_16:g.4822C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-133C= ENSP00000512234.1:n.-133C=
ENST00000696039.1:n.309C=
ENST00000696062.1:c.96+186C= ENSP00000512365.1:n.96+186C=
ENST00000696064.1:c.-130C= ENSP00000512367.1:n.-130C=
ENST00000696065.1:c.-133C= ENSP00000512368.1:n.-133C=
ENST00000535573.1:n.320C=
ENST00000536076.1:n.201C=
XM_011528479.1:c.-269C= XP_011526781.1:n.-269C=