Canonical Allele Identifier: CA2365869180
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651948C= , CM000682.2:g.44651948C= GRCh38
NC_000020.10:g.43280589C= , CM000682.1:g.43280589C= GRCh37
NC_000020.9:g.42714003C= NCBI36
NG_007385.1:g.4788G= , LRG_16:g.4788G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-167G= ENSP00000512234.1:n.-167G=
ENST00000696039.1:n.275G=
ENST00000696062.1:c.96+152G= ENSP00000512365.1:n.96+152G=
ENST00000696064.1:c.-164G= ENSP00000512367.1:n.-164G=
ENST00000535573.1:n.286G=
ENST00000536076.1:n.167G=
XM_011528479.1:c.-303G= XP_011526781.1:n.-303G=