Canonical Allele Identifier: CA2365869198
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651981C= , CM000682.2:g.44651981C= GRCh38
NC_000020.10:g.43280622C= , CM000682.1:g.43280622C= GRCh37
NC_000020.9:g.42714036C= NCBI36
NG_007385.1:g.4755G= , LRG_16:g.4755G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-200G= ENSP00000512234.1:n.-200G=
ENST00000696039.1:n.242G=
ENST00000696062.1:c.96+119G= ENSP00000512365.1:n.96+119G=
ENST00000696064.1:c.-197G= ENSP00000512367.1:n.-197G=
ENST00000535573.1:n.253G=
ENST00000536076.1:n.134G=
XM_011528479.1:c.-336G= XP_011526781.1:n.-336G=