Canonical Allele Identifier: CA2652992558
Gene: ADA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651820G>A , CM000682.2:g.44651820G>A GRCh38
NC_000020.10:g.43280461G>A , CM000682.1:g.43280461G>A GRCh37
NC_000020.9:g.42713875G>A NCBI36
NG_007385.1:g.4916C>T , LRG_16:g.4916C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+82C>T ENSP00000512234.1:n.-121+82C>T
ENST00000696039.1:n.321+82C>T
ENST00000696062.1:c.96+280C>T ENSP00000512365.1:n.96+280C>T
ENST00000696064.1:c.-118+82C>T ENSP00000512367.1:n.-118+82C>T
ENST00000696065.1:c.-121+82C>T ENSP00000512368.1:n.-121+82C>T
ENST00000535573.1:n.332+82C>T
ENST00000536076.1:n.213+82C>T
XM_011528479.1:c.-257+82C>T XP_011526781.1:n.-257+82C>T