Canonical Allele Identifier: CA2365869187
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651960C= , CM000682.2:g.44651960C= GRCh38
NC_000020.10:g.43280601C= , CM000682.1:g.43280601C= GRCh37
NC_000020.9:g.42714015C= NCBI36
NG_007385.1:g.4776G= , LRG_16:g.4776G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-179G= ENSP00000512234.1:n.-179G=
ENST00000696039.1:n.263G=
ENST00000696062.1:c.96+140G= ENSP00000512365.1:n.96+140G=
ENST00000696064.1:c.-176G= ENSP00000512367.1:n.-176G=
ENST00000535573.1:n.274G=
ENST00000536076.1:n.155G=
XM_011528479.1:c.-315G= XP_011526781.1:n.-315G=