Canonical Allele Identifier: CA1888027585
Gene: IL2RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6059720C= , CM000672.2:g.6059720C= GRCh38
NC_000010.10:g.6101683C= , CM000672.1:g.6101683C= GRCh37
NC_000010.9:g.6141689C= NCBI36
NG_007403.1:g.7590G= , LRG_73:g.7590G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447847.2:c.64+2368G= ENSP00000402024.2:n.64+2368G=
ENST00000697424.1:c.64+2368G= ENSP00000513307.1:n.64+2368G=
ENST00000379959.8:c.64+2368G= MANE Select ENSP00000369293.3:n.64+2368G=
ENST00000644262.1:n.279+2372G=
ENST00000256876.10:c.64+2368G= ENSP00000256876.6:n.64+2368G=
ENST00000379954.5:c.64+2368G= ENSP00000369287.1:n.64+2368G=
ENST00000379959.7:c.64+2368G= ENSP00000369293.3:n.64+2368G=
NM_000417.2:c.64+2368G= , LRG_73t1:c.64+2368G= NP_000408.1:n.64+2368G=
NM_001308242.1:c.64+2368G= NP_001295171.1:n.64+2368G=
NM_001308243.1:c.64+2368G= NP_001295172.1:n.64+2368G=
NM_000417.3:c.64+2368G= MANE Select NP_000408.1:n.64+2368G=
NM_001308242.2:c.64+2368G= NP_001295171.1:n.64+2368G=
NM_001308243.2:c.64+2368G= NP_001295172.1:n.64+2368G=