Canonical Allele Identifier: CA2365869183
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651951C= , CM000682.2:g.44651951C= GRCh38
NC_000020.10:g.43280592C= , CM000682.1:g.43280592C= GRCh37
NC_000020.9:g.42714006C= NCBI36
NG_007385.1:g.4785G= , LRG_16:g.4785G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-170G= ENSP00000512234.1:n.-170G=
ENST00000696039.1:n.272G=
ENST00000696062.1:c.96+149G= ENSP00000512365.1:n.96+149G=
ENST00000696064.1:c.-167G= ENSP00000512367.1:n.-167G=
ENST00000535573.1:n.283G=
ENST00000536076.1:n.164G=
XM_011528479.1:c.-306G= XP_011526781.1:n.-306G=