Canonical Allele Identifier: CA1888032242

Gene: IL2RA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6057071C= , CM000672.2:g.6057071C=	GRCh38
NC_000010.10:g.6099034C= , CM000672.1:g.6099034C=	GRCh37
NC_000010.9:g.6139040C=	NCBI36
NG_007403.1:g.10239G= , LRG_73:g.10239G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447847.2:c.64+5017G=	ENSP00000402024.2:n.64+5017G=
ENST00000697424.1:c.64+5017G=	ENSP00000513307.1:n.64+5017G=
ENST00000379959.8:c.64+5017G= MANE Select	ENSP00000369293.3:n.64+5017G=
ENST00000644262.1:n.279+5021G=
ENST00000256876.10:c.64+5017G=	ENSP00000256876.6:n.64+5017G=
ENST00000379954.5:c.64+5017G=	ENSP00000369287.1:n.64+5017G=
ENST00000379959.7:c.64+5017G=	ENSP00000369293.3:n.64+5017G=
NM_000417.2:c.64+5017G= , LRG_73t1:c.64+5017G=	NP_000408.1:n.64+5017G=
NM_001308242.1:c.64+5017G=	NP_001295171.1:n.64+5017G=
NM_001308243.1:c.64+5017G=	NP_001295172.1:n.64+5017G=
NM_000417.3:c.64+5017G= MANE Select	NP_000408.1:n.64+5017G=
NM_001308242.2:c.64+5017G=	NP_001295171.1:n.64+5017G=
NM_001308243.2:c.64+5017G=	NP_001295172.1:n.64+5017G=