Canonical Allele Identifier: CA2695235077
Gene: IL2RG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71110629del , CM000685.2:g.71110629del GRCh38
NC_000023.10:g.70330479del , CM000685.1:g.70330479del GRCh37
NC_000023.9:g.70247204del NCBI36
NG_009088.1:g.5927del , LRG_150:g.5927del
NG_021141.1:g.1162del

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.331del ENSP00000421262.2:p.Ile111SerfsTer?
ENST00000696903.1:n.382del
ENST00000374202.7:c.331del MANE Select ENSP00000363318.3:p.Ile111SerfsTer?
ENST00000642473.1:n.695del
ENST00000644022.1:n.737del
ENST00000644708.1:n.737del
ENST00000644911.1:n.737del
ENST00000645266.1:c.331del ENSP00000493734.1:p.Ile111SerfsTer?
ENST00000645518.1:c.331del ENSP00000493986.1:p.Ile111SerfsTer?
ENST00000646106.1:c.331del ENSP00000496437.1:p.Ile111SerfsTer?
ENST00000646505.1:c.331del ENSP00000496673.1:p.Ile111SerfsTer?
ENST00000647492.1:c.331del ENSP00000495340.1:p.Ile111SerfsTer?
ENST00000276110.6:n.716del
ENST00000374188.7:c.-386del ENSP00000363303.3:n.-386del
ENST00000374202.6:c.331del ENSP00000363318.2:p.Ile111SerfsTer?
ENST00000456850.6:c.24+798del ENSP00000388967.2:n.24+798del
ENST00000464642.5:c.199del ENSP00000425233.1:p.Ile67SerfsTer?
ENST00000473378.1:c.268del ENSP00000423601.1:p.Ile90SerfsTer?
ENST00000487883.1:c.295del ENSP00000423966.1:p.Ile99SerfsTer?
ENST00000512747.3:n.398del
NM_000206.2:c.331del , LRG_150t1:c.331del NP_000197.1:p.Ile111SerfsTer?
NM_000206.3:c.331del MANE Select NP_000197.1:p.Ile111SerfsTer?