Canonical Allele Identifier: CA2365869077
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651798G= , CM000682.2:g.44651798G= GRCh38
NC_000020.10:g.43280439G= , CM000682.1:g.43280439G= GRCh37
NC_000020.9:g.42713853G= NCBI36
NG_007385.1:g.4938C= , LRG_16:g.4938C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+104C= ENSP00000512234.1:n.-121+104C=
ENST00000696039.1:n.321+104C=
ENST00000696062.1:c.96+302C= ENSP00000512365.1:n.96+302C=
ENST00000696064.1:c.-118+104C= ENSP00000512367.1:n.-118+104C=
ENST00000696065.1:c.-121+104C= ENSP00000512368.1:n.-121+104C=
ENST00000535573.1:n.332+104C=
ENST00000536076.1:n.213+104C=
XM_011528479.1:c.-257+104C= XP_011526781.1:n.-257+104C=