Canonical Allele Identifier: CA3174154837
Community Standard Title: NM_000417.3(IL2RA):c.692A= (p.Glu231=)
Gene: IL2RA HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_000417.3:c.692A= MANE Select NP_000408.1:p.Glu231=
ENST00000379959.8:c.692A= MANE Select ENSP00000369293.3:p.Glu231=
NM_000417.2:c.692A= , LRG_73t1:c.692A= NP_000408.1:p.Glu231=
NM_001308242.1:c.476A= NP_001295171.1:p.Glu159=
NM_001308242.2:c.476A= NP_001295171.1:p.Glu159=
NM_001308243.1:c.404A= NP_001295172.1:p.Glu135=
NM_001308243.2:c.404A= NP_001295172.1:p.Glu135=
ENST00000256876.10:c.665A= ENSP00000256876.6:p.Glu222=
ENST00000379954.5:c.476A= ENSP00000369287.1:p.Glu159=
ENST00000379959.7:c.692A= ENSP00000369293.3:p.Glu231=
ENST00000447847.1:c.316A=
ENST00000447847.2:c.404A= ENSP00000402024.2:p.Glu135=
ENST00000649218.1:n.507A=
ENST00000697424.1:c.620A= ENSP00000513307.1:p.Glu207=