Canonical Allele Identifier: CA10602390
Gene: IL2RA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6019463dup , CM000672.2:g.6019463dup GRCh38
NC_000010.10:g.6061426dup , CM000672.1:g.6061426dup GRCh37
NC_000010.9:g.6101432dup NCBI36
NG_007403.1:g.47847dup , LRG_73:g.47847dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000447847.2:c.404dup ENSP00000402024.2:p.Thr136AspfsTer?
ENST00000697424.1:c.620dup ENSP00000513307.1:p.Thr208AspfsTer?
ENST00000379959.8:c.692dup MANE Select ENSP00000369293.3:p.Thr232AspfsTer?
ENST00000649218.1:n.507dup
ENST00000256876.10:c.665dup ENSP00000256876.6:p.Thr223AspfsTer?
ENST00000379954.5:c.476dup ENSP00000369287.1:p.Thr160AspfsTer?
ENST00000379959.7:c.692dup ENSP00000369293.3:p.Thr232AspfsTer?
ENST00000447847.1:c.316dup
NM_000417.2:c.692dup , LRG_73t1:c.692dup NP_000408.1:p.Thr232AspfsTer?
NM_001308242.1:c.476dup NP_001295171.1:p.Thr160AspfsTer?
NM_001308243.1:c.404dup NP_001295172.1:p.Thr136AspfsTer?
NM_000417.3:c.692dup MANE Select NP_000408.1:p.Thr232AspfsTer?
NM_001308242.2:c.476dup NP_001295171.1:p.Thr160AspfsTer?
NM_001308243.2:c.404dup NP_001295172.1:p.Thr136AspfsTer?
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