Canonical Allele Identifier: CA2577406114
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651779C>A , CM000682.2:g.44651779C>A GRCh38
NC_000020.10:g.43280420C>A , CM000682.1:g.43280420C>A GRCh37
NC_000020.9:g.42713834C>A NCBI36
NG_007385.1:g.4957G>T , LRG_16:g.4957G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+123G>T ENSP00000512234.1:n.-121+123G>T
ENST00000696039.1:n.321+123G>T
ENST00000696062.1:c.96+321G>T ENSP00000512365.1:n.96+321G>T
ENST00000696064.1:c.-118+123G>T ENSP00000512367.1:n.-118+123G>T
ENST00000696065.1:c.-121+123G>T ENSP00000512368.1:n.-121+123G>T
ENST00000535573.1:n.332+123G>T
ENST00000536076.1:n.213+123G>T
XM_011528479.1:c.-257+123G>T XP_011526781.1:n.-257+123G>T