Canonical Allele Identifier: CA2652992664
Gene: ADA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651912_44651936del , CM000682.2:g.44651912_44651936del GRCh38
NC_000020.10:g.43280553_43280577del , CM000682.1:g.43280553_43280577del GRCh37
NC_000020.9:g.42713967_42713991del NCBI36
NG_007385.1:g.4807_4831del , LRG_16:g.4807_4831del

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-148_-124del ENSP00000512234.1:n.-148_-124del
ENST00000696039.1:n.294_318del
ENST00000696062.1:c.96+171_96+195del ENSP00000512365.1:n.96+171_96+195del
ENST00000696064.1:c.-145_-121del ENSP00000512367.1:n.-145_-121del
ENST00000535573.1:n.305_329del
ENST00000536076.1:n.186_210del
XM_011528479.1:c.-284_-260del XP_011526781.1:n.-284_-260del