Canonical Allele Identifier: CA2365869167
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651932G= , CM000682.2:g.44651932G= GRCh38
NC_000020.10:g.43280573G= , CM000682.1:g.43280573G= GRCh37
NC_000020.9:g.42713987G= NCBI36
NG_007385.1:g.4804C= , LRG_16:g.4804C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-151C= ENSP00000512234.1:n.-151C=
ENST00000696039.1:n.291C=
ENST00000696062.1:c.96+168C= ENSP00000512365.1:n.96+168C=
ENST00000696064.1:c.-148C= ENSP00000512367.1:n.-148C=
ENST00000535573.1:n.302C=
ENST00000536076.1:n.183C=
XM_011528479.1:c.-287C= XP_011526781.1:n.-287C=