Canonical Allele Identifier: CA2821721039

Gene: IL2RG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110796_71110797del , CM000685.2:g.71110796_71110797del	GRCh38
NC_000023.10:g.70330646_70330647del , CM000685.1:g.70330646_70330647del	GRCh37
NC_000023.9:g.70247371_70247372del	NCBI36
NG_009088.1:g.5757_5758del , LRG_150:g.5757_5758del
NG_021141.1:g.992_993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.269+100_269+101del	ENSP00000421262.2:n.269+100_269+101del
ENST00000696903.1:n.320+100_320+101del
ENST00000374202.7:c.269+100_269+101del MANE Select	ENSP00000363318.3:n.269+100_269+101del
ENST00000642473.1:n.633+100_633+101del
ENST00000644022.1:n.675+100_675+101del
ENST00000644708.1:n.675+100_675+101del
ENST00000644911.1:n.675+100_675+101del
ENST00000645266.1:c.269+100_269+101del	ENSP00000493734.1:n.269+100_269+101del
ENST00000645518.1:c.269+100_269+101del	ENSP00000493986.1:n.269+100_269+101del
ENST00000646106.1:c.269+100_269+101del	ENSP00000496437.1:n.269+100_269+101del
ENST00000646505.1:c.269+100_269+101del	ENSP00000496673.1:n.269+100_269+101del
ENST00000647492.1:c.269+100_269+101del	ENSP00000495340.1:n.269+100_269+101del
ENST00000276110.6:n.654+100_654+101del
ENST00000374188.7:c.-448+100_-448+101del	ENSP00000363303.3:n.-448+100_-448+101del
ENST00000374202.6:c.269+100_269+101del	ENSP00000363318.2:n.269+100_269+101del
ENST00000456850.6:c.24+628_24+629del	ENSP00000388967.2:n.24+628_24+629del
ENST00000464642.5:c.137+100_137+101del	ENSP00000425233.1:n.137+100_137+101del
ENST00000473378.1:c.206+100_206+101del	ENSP00000423601.1:n.206+100_206+101del
ENST00000487883.1:c.233+100_233+101del	ENSP00000423966.1:n.233+100_233+101del
ENST00000512747.3:n.336+100_336+101del
NM_000206.2:c.269+100_269+101del , LRG_150t1:c.269+100_269+101del	NP_000197.1:n.269+100_269+101del
NM_000206.3:c.269+100_269+101del MANE Select	NP_000197.1:n.269+100_269+101del