Canonical Allele Identifier: CA2652992670
Gene: ADA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651914_44651915del , CM000682.2:g.44651914_44651915del GRCh38
NC_000020.10:g.43280555_43280556del , CM000682.1:g.43280555_43280556del GRCh37
NC_000020.9:g.42713969_42713970del NCBI36
NG_007385.1:g.4827_4828del , LRG_16:g.4827_4828del

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-128_-127del ENSP00000512234.1:n.-128_-127del
ENST00000696039.1:n.314_315del
ENST00000696062.1:c.96+191_96+192del ENSP00000512365.1:n.96+191_96+192del
ENST00000696064.1:c.-125_-124del ENSP00000512367.1:n.-125_-124del
ENST00000696065.1:c.-128_-127del ENSP00000512368.1:n.-128_-127del
ENST00000535573.1:n.325_326del
ENST00000536076.1:n.206_207del
XM_011528479.1:c.-264_-263del XP_011526781.1:n.-264_-263del