Canonical Allele Identifier: CA202288776
Community Standard Title: NM_000417.3(IL2RA):c.*55T>C
Gene: IL2RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6012817A>G , CM000672.2:g.6012817A>G GRCh38
NC_000010.10:g.6054780A>G , CM000672.1:g.6054780A>G GRCh37
NC_000010.9:g.6094786A>G NCBI36
NG_007403.1:g.54493T>C , LRG_73:g.54493T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000417.3:c.*55T>C MANE Select NP_000408.1:n.*55T>C
ENST00000379959.8:c.*55T>C MANE Select ENSP00000369293.3:n.*55T>C
NM_000417.2:c.*55T>C , LRG_73t1:c.*55T>C NP_000408.1:n.*55T>C
NM_001308242.1:c.*55T>C NP_001295171.1:n.*55T>C
NM_001308242.2:c.*55T>C NP_001295171.1:n.*55T>C
NM_001308243.1:c.*55T>C NP_001295172.1:n.*55T>C
NM_001308243.2:c.*55T>C NP_001295172.1:n.*55T>C
ENST00000256876.10:c.*55T>C ENSP00000256876.6:n.*55T>C
ENST00000379954.5:c.*55T>C ENSP00000369287.1:n.*55T>C
ENST00000379959.7:c.*55T>C ENSP00000369293.3:n.*55T>C
ENST00000447847.2:c.*55T>C ENSP00000402024.2:n.*55T>C
ENST00000649218.1:n.689T>C