Canonical Allele Identifier: CA2365869149
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651910G= , CM000682.2:g.44651910G= GRCh38
NC_000020.10:g.43280551G= , CM000682.1:g.43280551G= GRCh37
NC_000020.9:g.42713965G= NCBI36
NG_007385.1:g.4826C= , LRG_16:g.4826C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-129C= ENSP00000512234.1:n.-129C=
ENST00000696039.1:n.313C=
ENST00000696062.1:c.96+190C= ENSP00000512365.1:n.96+190C=
ENST00000696064.1:c.-126C= ENSP00000512367.1:n.-126C=
ENST00000696065.1:c.-129C= ENSP00000512368.1:n.-129C=
ENST00000535573.1:n.324C=
ENST00000536076.1:n.205C=
XM_011528479.1:c.-265C= XP_011526781.1:n.-265C=