Canonical Allele Identifier: CA1888011799
Gene: IL2RA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6011161A= , CM000672.2:g.6011161A= GRCh38
NC_000010.10:g.6053124A= , CM000672.1:g.6053124A= GRCh37
NC_000010.9:g.6093130A= NCBI36
NG_007403.1:g.56149T= , LRG_73:g.56149T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379959.8:c.*1711T= MANE Select ENSP00000369293.3:n.*1711T=
ENST00000649218.1:n.2345T=
ENST00000379959.7:c.*1711T= ENSP00000369293.3:n.*1711T=
NM_000417.2:c.*1711T= , LRG_73t1:c.*1711T= NP_000408.1:n.*1711T=
NM_001308242.1:c.*1711T= NP_001295171.1:n.*1711T=
NM_001308243.1:c.*1711T= NP_001295172.1:n.*1711T=
NM_000417.3:c.*1711T= MANE Select NP_000408.1:n.*1711T=
NM_001308242.2:c.*1711T= NP_001295171.1:n.*1711T=
NM_001308243.2:c.*1711T= NP_001295172.1:n.*1711T=
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