Canonical Allele Identifier: CA1888026529

Gene: IL2RA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6058762G= , CM000672.2:g.6058762G=	GRCh38
NC_000010.10:g.6100725G= , CM000672.1:g.6100725G=	GRCh37
NC_000010.9:g.6140731G=	NCBI36
NG_007403.1:g.8548C= , LRG_73:g.8548C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000417.3:c.64+3326C= MANE Select	NP_000408.1:n.64+3326C=
ENST00000379959.8:c.64+3326C= MANE Select	ENSP00000369293.3:n.64+3326C=
NM_000417.2:c.64+3326C= , LRG_73t1:c.64+3326C=	NP_000408.1:n.64+3326C=
NM_001308242.1:c.64+3326C=	NP_001295171.1:n.64+3326C=
NM_001308242.2:c.64+3326C=	NP_001295171.1:n.64+3326C=
NM_001308243.1:c.64+3326C=	NP_001295172.1:n.64+3326C=
NM_001308243.2:c.64+3326C=	NP_001295172.1:n.64+3326C=
ENST00000256876.10:c.64+3326C=	ENSP00000256876.6:n.64+3326C=
ENST00000379954.5:c.64+3326C=	ENSP00000369287.1:n.64+3326C=
ENST00000379959.7:c.64+3326C=	ENSP00000369293.3:n.64+3326C=
ENST00000447847.2:c.64+3326C=	ENSP00000402024.2:n.64+3326C=
ENST00000644262.1:n.279+3330C=
ENST00000697424.1:c.64+3326C=	ENSP00000513307.1:n.64+3326C=