Canonical Allele Identifier: CA2365869126
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651866G= , CM000682.2:g.44651866G= GRCh38
NC_000020.10:g.43280507G= , CM000682.1:g.43280507G= GRCh37
NC_000020.9:g.42713921G= NCBI36
NG_007385.1:g.4870C= , LRG_16:g.4870C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+36C= ENSP00000512234.1:n.-121+36C=
ENST00000696039.1:n.321+36C=
ENST00000696062.1:c.96+234C= ENSP00000512365.1:n.96+234C=
ENST00000696064.1:c.-118+36C= ENSP00000512367.1:n.-118+36C=
ENST00000696065.1:c.-121+36C= ENSP00000512368.1:n.-121+36C=
ENST00000535573.1:n.332+36C=
ENST00000536076.1:n.213+36C=
XM_011528479.1:c.-257+36C= XP_011526781.1:n.-257+36C=