Canonical Allele Identifier: CA2365869164
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651928G= , CM000682.2:g.44651928G= GRCh38
NC_000020.10:g.43280569G= , CM000682.1:g.43280569G= GRCh37
NC_000020.9:g.42713983G= NCBI36
NG_007385.1:g.4808C= , LRG_16:g.4808C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-147C= ENSP00000512234.1:n.-147C=
ENST00000696039.1:n.295C=
ENST00000696062.1:c.96+172C= ENSP00000512365.1:n.96+172C=
ENST00000696064.1:c.-144C= ENSP00000512367.1:n.-144C=
ENST00000535573.1:n.306C=
ENST00000536076.1:n.187C=
XM_011528479.1:c.-283C= XP_011526781.1:n.-283C=