Canonical Allele Identifier: CA2652992381
Gene: ADA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651679_44651708del , CM000682.2:g.44651679_44651708del GRCh38
NC_000020.10:g.43280320_43280349del , CM000682.1:g.43280320_43280349del GRCh37
NC_000020.9:g.42713734_42713763del NCBI36
NG_007385.1:g.5038_5067del , LRG_16:g.5038_5067del

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+204_-121+233del ENSP00000512234.1:n.-121+204_-121+233del
ENST00000537820.2:c.-91_-62del ENSP00000441818.1:n.-91_-62del
ENST00000695949.1:c.-91_-62del ENSP00000512281.1:n.-91_-62del
ENST00000695993.1:c.-91_-62del ENSP00000512316.1:n.-91_-62del
ENST00000696006.1:c.-91_-62del ENSP00000512325.1:n.-91_-62del
ENST00000696009.1:n.21_50del
ENST00000696010.1:n.23_52del
ENST00000696039.1:n.321+204_321+233del
ENST00000696059.1:c.-91_-62del ENSP00000512362.1:n.-91_-62del
ENST00000696060.1:c.-91_-62del ENSP00000512363.1:n.-91_-62del
ENST00000696061.1:c.-91_-62del ENSP00000512364.1:n.-91_-62del
ENST00000696062.1:c.96+402_96+431del ENSP00000512365.1:n.96+402_96+431del
ENST00000696064.1:c.-118+204_-118+233del ENSP00000512367.1:n.-118+204_-118+233del
ENST00000696065.1:c.-121+204_-121+233del ENSP00000512368.1:n.-121+204_-121+233del
ENST00000696076.1:c.-91_-62del ENSP00000512375.1:n.-91_-62del
ENST00000696077.1:c.-91_-62del ENSP00000512376.1:n.-91_-62del
ENST00000696078.1:c.-91_-62del ENSP00000512377.1:n.-91_-62del
ENST00000696080.1:c.-91_-62del ENSP00000512379.1:n.-91_-62del
ENST00000696084.1:n.11_40del
ENST00000372874.8:c.-91_-62del ENSP00000361965.4:n.-91_-62del
ENST00000535573.1:n.332+204_332+233del
ENST00000536076.1:n.213+204_213+233del
NM_000022.2:c.-91_-62del , LRG_16t1:c.-91_-62del NP_000013.2:n.-91_-62del
XM_011528479.1:c.-257+204_-257+233del XP_011526781.1:n.-257+204_-257+233del
NM_000022.3:c.-91_-62del NP_000013.2:n.-91_-62del
NM_001322050.1:c.-380_-351del NP_001308979.1:n.-380_-351del
NM_001322051.1:c.-91_-62del NP_001308980.1:n.-91_-62del
NR_136160.1:n.61_90del