Canonical Allele Identifier: CA2436348758

Gene: IL2RG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110982A= , CM000685.2:g.71110982A=	GRCh38
NC_000023.10:g.70330832A= , CM000685.1:g.70330832A=	GRCh37
NC_000023.9:g.70247557A=	NCBI36
NG_009088.1:g.5572T= , LRG_150:g.5572T=
NG_021141.1:g.807T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.184T=	ENSP00000421262.2:p.Cys62=
ENST00000696903.1:n.235T=
ENST00000374202.7:c.184T= MANE Select	ENSP00000363318.3:p.Cys62=
ENST00000642473.1:n.548T=
ENST00000644022.1:n.590T=
ENST00000644708.1:n.590T=
ENST00000644911.1:n.590T=
ENST00000645266.1:c.184T=	ENSP00000493734.1:p.Cys62=
ENST00000645518.1:c.184T=	ENSP00000493986.1:p.Cys62=
ENST00000646106.1:c.184T=	ENSP00000496437.1:p.Cys62=
ENST00000646505.1:c.184T=	ENSP00000496673.1:p.Cys62=
ENST00000647492.1:c.184T=	ENSP00000495340.1:p.Cys62=
ENST00000276110.6:n.569T=
ENST00000374188.7:c.-533T=	ENSP00000363303.3:n.-533T=
ENST00000374202.6:c.184T=	ENSP00000363318.2:p.Cys62=
ENST00000456850.6:c.24+443T=	ENSP00000388967.2:n.24+443T=
ENST00000464642.5:c.52T=	ENSP00000425233.1:p.Cys18=
ENST00000473378.1:c.121T=	ENSP00000423601.1:p.Cys41=
ENST00000487883.1:c.148T=	ENSP00000423966.1:p.Cys50=
ENST00000512747.3:n.251T=
NM_000206.2:c.184T= , LRG_150t1:c.184T=	NP_000197.1:p.Cys62=
NM_000206.3:c.184T= MANE Select	NP_000197.1:p.Cys62=