Canonical Allele Identifier: CA2365869146
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651906G= , CM000682.2:g.44651906G= GRCh38
NC_000020.10:g.43280547G= , CM000682.1:g.43280547G= GRCh37
NC_000020.9:g.42713961G= NCBI36
NG_007385.1:g.4830C= , LRG_16:g.4830C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-125C= ENSP00000512234.1:n.-125C=
ENST00000696039.1:n.317C=
ENST00000696062.1:c.96+194C= ENSP00000512365.1:n.96+194C=
ENST00000696064.1:c.-122C= ENSP00000512367.1:n.-122C=
ENST00000696065.1:c.-125C= ENSP00000512368.1:n.-125C=
ENST00000535573.1:n.328C=
ENST00000536076.1:n.209C=
XM_011528479.1:c.-261C= XP_011526781.1:n.-261C=