Canonical Allele Identifier: CA1888027556
Gene: IL2RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6059703G= , CM000672.2:g.6059703G= GRCh38
NC_000010.10:g.6101666G= , CM000672.1:g.6101666G= GRCh37
NC_000010.9:g.6141672G= NCBI36
NG_007403.1:g.7607C= , LRG_73:g.7607C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447847.2:c.64+2385C= ENSP00000402024.2:n.64+2385C=
ENST00000697424.1:c.64+2385C= ENSP00000513307.1:n.64+2385C=
ENST00000379959.8:c.64+2385C= MANE Select ENSP00000369293.3:n.64+2385C=
ENST00000644262.1:n.279+2389C=
ENST00000256876.10:c.64+2385C= ENSP00000256876.6:n.64+2385C=
ENST00000379954.5:c.64+2385C= ENSP00000369287.1:n.64+2385C=
ENST00000379959.7:c.64+2385C= ENSP00000369293.3:n.64+2385C=
NM_000417.2:c.64+2385C= , LRG_73t1:c.64+2385C= NP_000408.1:n.64+2385C=
NM_001308242.1:c.64+2385C= NP_001295171.1:n.64+2385C=
NM_001308243.1:c.64+2385C= NP_001295172.1:n.64+2385C=
NM_000417.3:c.64+2385C= MANE Select NP_000408.1:n.64+2385C=
NM_001308242.2:c.64+2385C= NP_001295171.1:n.64+2385C=
NM_001308243.2:c.64+2385C= NP_001295172.1:n.64+2385C=