Canonical Allele Identifier: CA2365869189
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651967C= , CM000682.2:g.44651967C= GRCh38
NC_000020.10:g.43280608C= , CM000682.1:g.43280608C= GRCh37
NC_000020.9:g.42714022C= NCBI36
NG_007385.1:g.4769G= , LRG_16:g.4769G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-186G= ENSP00000512234.1:n.-186G=
ENST00000696039.1:n.256G=
ENST00000696062.1:c.96+133G= ENSP00000512365.1:n.96+133G=
ENST00000696064.1:c.-183G= ENSP00000512367.1:n.-183G=
ENST00000535573.1:n.267G=
ENST00000536076.1:n.148G=
XM_011528479.1:c.-322G= XP_011526781.1:n.-322G=