Canonical Allele Identifier: CA2365869202
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651990C= , CM000682.2:g.44651990C= GRCh38
NC_000020.10:g.43280631C= , CM000682.1:g.43280631C= GRCh37
NC_000020.9:g.42714045C= NCBI36
NG_007385.1:g.4746G= , LRG_16:g.4746G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-209G= ENSP00000512234.1:n.-209G=
ENST00000696039.1:n.233G=
ENST00000696062.1:c.96+110G= ENSP00000512365.1:n.96+110G=
ENST00000696064.1:c.-206G= ENSP00000512367.1:n.-206G=
ENST00000535573.1:n.244G=
ENST00000536076.1:n.125G=
XM_011528479.1:c.-345G= XP_011526781.1:n.-345G=