Canonical Allele Identifier: CA2365869178
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651945C= , CM000682.2:g.44651945C= GRCh38
NC_000020.10:g.43280586C= , CM000682.1:g.43280586C= GRCh37
NC_000020.9:g.42714000C= NCBI36
NG_007385.1:g.4791G= , LRG_16:g.4791G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-164G= ENSP00000512234.1:n.-164G=
ENST00000696039.1:n.278G=
ENST00000696062.1:c.96+155G= ENSP00000512365.1:n.96+155G=
ENST00000696064.1:c.-161G= ENSP00000512367.1:n.-161G=
ENST00000535573.1:n.289G=
ENST00000536076.1:n.170G=
XM_011528479.1:c.-300G= XP_011526781.1:n.-300G=