Canonical Allele Identifier: CA2436348614

Gene: IL2RG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110559C= , CM000685.2:g.71110559C=	GRCh38
NC_000023.10:g.70330409C= , CM000685.1:g.70330409C=	GRCh37
NC_000023.9:g.70247134C=	NCBI36
NG_009088.1:g.5995G= , LRG_150:g.5995G=
NG_021141.1:g.1230G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.399G=	ENSP00000421262.2:p.Gln133=
ENST00000696903.1:n.450G=
ENST00000374202.7:c.399G= MANE Select	ENSP00000363318.3:p.Gln133=
ENST00000642473.1:n.763G=
ENST00000644022.1:n.805G=
ENST00000644708.1:n.805G=
ENST00000644911.1:n.805G=
ENST00000645266.1:c.399G=	ENSP00000493734.1:p.Gln133=
ENST00000645518.1:c.399G=	ENSP00000493986.1:p.Gln133=
ENST00000646106.1:c.399G=	ENSP00000496437.1:p.Gln133=
ENST00000646505.1:c.399G=	ENSP00000496673.1:p.Gln133=
ENST00000647492.1:c.399G=	ENSP00000495340.1:p.Gln133=
ENST00000276110.6:n.784G=
ENST00000374188.7:c.-318G=	ENSP00000363303.3:n.-318G=
ENST00000374202.6:c.399G=	ENSP00000363318.2:p.Gln133=
ENST00000456850.6:c.24+866G=	ENSP00000388967.2:n.24+866G=
ENST00000464642.5:c.267G=	ENSP00000425233.1:p.Gln89=
ENST00000487883.1:c.363G=	ENSP00000423966.1:p.Gln121=
ENST00000512747.3:n.466G=
NM_000206.2:c.399G= , LRG_150t1:c.399G=	NP_000197.1:p.Gln133=
NM_000206.3:c.399G= MANE Select	NP_000197.1:p.Gln133=