Canonical Allele Identifier: CA1888011730
Gene: IL2RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6010983T= , CM000672.2:g.6010983T= GRCh38
NC_000010.10:g.6052946T= , CM000672.1:g.6052946T= GRCh37
NC_000010.9:g.6092952T= NCBI36
NG_007403.1:g.56327A= , LRG_73:g.56327A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379959.8:c.*1889A= MANE Select ENSP00000369293.3:n.*1889A=
ENST00000649218.1:n.2523A=
ENST00000379959.7:c.*1889A= ENSP00000369293.3:n.*1889A=
NM_000417.2:c.*1889A= , LRG_73t1:c.*1889A= NP_000408.1:n.*1889A=
NM_001308242.1:c.*1889A= NP_001295171.1:n.*1889A=
NM_001308243.1:c.*1889A= NP_001295172.1:n.*1889A=
NM_000417.3:c.*1889A= MANE Select NP_000408.1:n.*1889A=
NM_001308242.2:c.*1889A= NP_001295171.1:n.*1889A=
NM_001308243.2:c.*1889A= NP_001295172.1:n.*1889A=