Canonical Allele Identifier: CA2365869065
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651784_44651805delinsTCGCCGGAGCCCCCGCCCCGCC , CM000682.2:g.44651784_44651805delinsTCGCCGGAGCCCCCGCCCCGCC GRCh38
NC_000020.10:g.43280425_43280446delinsTCGCCGGAGCCCCCGCCCCGCC , CM000682.1:g.43280425_43280446delinsTCGCCGGAGCCCCCGCCCCGCC GRCh37
NC_000020.9:g.42713839_42713860delinsTCGCCGGAGCCCCCGCCCCGCC NCBI36
NG_007385.1:g.4931_4952delinsGGCGGGGCGGGGGCTCCGGCGA , LRG_16:g.4931_4952delinsGGCGGGGCGGGGGCTCCGGCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+97_-121+118delinsGGCGGGGCGGGGGCTCCGGCGA ENSP00000512234.1:n.-121+97_-121+118delinsGGCGGGGCGGGGGCTCCGG...
ENST00000696039.1:n.321+97_321+118delinsGGCGGGGCGGGGGCTCCGGCGA
ENST00000696062.1:c.96+295_96+316delinsGGCGGGGCGGGGGCTCCGGCGA ENSP00000512365.1:n.96+295_96+316delinsGGCGGGGCGGGGGCTCCGGCGA...
ENST00000696064.1:c.-118+97_-118+118delinsGGCGGGGCGGGGGCTCCGGCGA ENSP00000512367.1:n.-118+97_-118+118delinsGGCGGGGCGGGGGCTCCGG...
ENST00000696065.1:c.-121+97_-121+118delinsGGCGGGGCGGGGGCTCCGGCGA ENSP00000512368.1:n.-121+97_-121+118delinsGGCGGGGCGGGGGCTCCGG...
ENST00000535573.1:n.332+97_332+118delinsGGCGGGGCGGGGGCTCCGGCGA
ENST00000536076.1:n.213+97_213+118delinsGGCGGGGCGGGGGCTCCGGCGA
XM_011528479.1:c.-257+97_-257+118delinsGGCGGGGCGGGGGCTCCGGCGA XP_011526781.1:n.-257+97_-257+118delinsGGCGGGGCGGGGGCTCCGGCGA...