Canonical Allele Identifier: CA2436348717

Gene: IL2RG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110838_71110840delinsCTT , CM000685.2:g.71110838_71110840delinsCTT	GRCh38
NC_000023.10:g.70330688_70330690delinsCTT , CM000685.1:g.70330688_70330690delinsCTT	GRCh37
NC_000023.9:g.70247413_70247415delinsCTT	NCBI36
NG_009088.1:g.5714_5716delinsAAG , LRG_150:g.5714_5716delinsAAG
NG_021141.1:g.949_951delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.269+57_269+59delinsAAG	ENSP00000421262.2:n.269+57_269+59delinsAAG
ENST00000696903.1:n.320+57_320+59delinsAAG
ENST00000374202.7:c.269+57_269+59delinsAAG MANE Select	ENSP00000363318.3:n.269+57_269+59delinsAAG
ENST00000642473.1:n.633+57_633+59delinsAAG
ENST00000644022.1:n.675+57_675+59delinsAAG
ENST00000644708.1:n.675+57_675+59delinsAAG
ENST00000644911.1:n.675+57_675+59delinsAAG
ENST00000645266.1:c.269+57_269+59delinsAAG	ENSP00000493734.1:n.269+57_269+59delinsAAG
ENST00000645518.1:c.269+57_269+59delinsAAG	ENSP00000493986.1:n.269+57_269+59delinsAAG
ENST00000646106.1:c.269+57_269+59delinsAAG	ENSP00000496437.1:n.269+57_269+59delinsAAG
ENST00000646505.1:c.269+57_269+59delinsAAG	ENSP00000496673.1:n.269+57_269+59delinsAAG
ENST00000647492.1:c.269+57_269+59delinsAAG	ENSP00000495340.1:n.269+57_269+59delinsAAG
ENST00000276110.6:n.654+57_654+59delinsAAG
ENST00000374188.7:c.-448+57_-448+59delinsAAG	ENSP00000363303.3:n.-448+57_-448+59delinsAAG
ENST00000374202.6:c.269+57_269+59delinsAAG	ENSP00000363318.2:n.269+57_269+59delinsAAG
ENST00000456850.6:c.24+585_24+587delinsAAG	ENSP00000388967.2:n.24+585_24+587delinsAAG
ENST00000464642.5:c.137+57_137+59delinsAAG	ENSP00000425233.1:n.137+57_137+59delinsAAG
ENST00000473378.1:c.206+57_206+59delinsAAG	ENSP00000423601.1:n.206+57_206+59delinsAAG
ENST00000487883.1:c.233+57_233+59delinsAAG	ENSP00000423966.1:n.233+57_233+59delinsAAG
ENST00000512747.3:n.336+57_336+59delinsAAG
NM_000206.2:c.269+57_269+59delinsAAG , LRG_150t1:c.269+57_269+59delinsAAG	NP_000197.1:n.269+57_269+59delinsAAG
NM_000206.3:c.269+57_269+59delinsAAG MANE Select	NP_000197.1:n.269+57_269+59delinsAAG