Canonical Allele Identifier: CA2365869194
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651977C= , CM000682.2:g.44651977C= GRCh38
NC_000020.10:g.43280618C= , CM000682.1:g.43280618C= GRCh37
NC_000020.9:g.42714032C= NCBI36
NG_007385.1:g.4759G= , LRG_16:g.4759G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-196G= ENSP00000512234.1:n.-196G=
ENST00000696039.1:n.246G=
ENST00000696062.1:c.96+123G= ENSP00000512365.1:n.96+123G=
ENST00000696064.1:c.-193G= ENSP00000512367.1:n.-193G=
ENST00000535573.1:n.257G=
ENST00000536076.1:n.138G=
XM_011528479.1:c.-332G= XP_011526781.1:n.-332G=