Canonical Allele Identifier: CA2816478422
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651880C>A , CM000682.2:g.44651880C>A GRCh38
NC_000020.10:g.43280521C>A , CM000682.1:g.43280521C>A GRCh37
NC_000020.9:g.42713935C>A NCBI36
NG_007385.1:g.4856G>T , LRG_16:g.4856G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+22G>T ENSP00000512234.1:n.-121+22G>T
ENST00000696039.1:n.321+22G>T
ENST00000696062.1:c.96+220G>T ENSP00000512365.1:n.96+220G>T
ENST00000696064.1:c.-118+22G>T ENSP00000512367.1:n.-118+22G>T
ENST00000696065.1:c.-121+22G>T ENSP00000512368.1:n.-121+22G>T
ENST00000535573.1:n.332+22G>T
ENST00000536076.1:n.213+22G>T
XM_011528479.1:c.-257+22G>T XP_011526781.1:n.-257+22G>T