Canonical Allele Identifier: CA2436348172

Gene: IL2RG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71109268T= , CM000685.2:g.71109268T=	GRCh38
NC_000023.10:g.70329118T= , CM000685.1:g.70329118T=	GRCh37
NC_000023.9:g.70245843T=	NCBI36
NG_009088.1:g.7286A= , LRG_150:g.7286A=
NG_021141.1:g.2521A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.717A=	ENSP00000421262.2:p.Glu239=
ENST00000696903.1:n.768A=
ENST00000374202.7:c.717A= MANE Select	ENSP00000363318.3:p.Glu239=
ENST00000642473.1:n.1081A=
ENST00000644022.1:n.983A=
ENST00000644708.1:n.1123A=
ENST00000644911.1:n.1123A=
ENST00000645266.1:c.717A=	ENSP00000493734.1:p.Glu239=
ENST00000645518.1:c.717A=	ENSP00000493986.1:p.Glu239=
ENST00000646106.1:c.717A=	ENSP00000496437.1:p.Glu239=
ENST00000646505.1:c.717A=	ENSP00000496673.1:p.Glu239=
ENST00000647492.1:c.717A=	ENSP00000495340.1:p.Glu239=
ENST00000276110.6:n.1310A=
ENST00000374188.7:c.1A=	ENSP00000363303.3:p.Met1=
ENST00000374202.6:c.717A=	ENSP00000363318.2:p.Glu239=
ENST00000456850.6:c.147A=	ENSP00000388967.2:p.Glu49=
ENST00000464642.5:c.585A=	ENSP00000425233.1:p.Glu195=
ENST00000482750.5:c.130A=
ENST00000512747.3:n.644A=
NM_000206.2:c.717A= , LRG_150t1:c.717A=	NP_000197.1:p.Glu239=
NM_000206.3:c.717A= MANE Select	NP_000197.1:p.Glu239=