Canonical Allele Identifier: CA2436348744

Gene: IL2RG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110914G= , CM000685.2:g.71110914G=	GRCh38
NC_000023.10:g.70330764G= , CM000685.1:g.70330764G=	GRCh37
NC_000023.9:g.70247489G=	NCBI36
NG_009088.1:g.5640C= , LRG_150:g.5640C=
NG_021141.1:g.875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.252C=	ENSP00000421262.2:p.Asn84=
ENST00000696903.1:n.303C=
ENST00000374202.7:c.252C= MANE Select	ENSP00000363318.3:p.Asn84=
ENST00000642473.1:n.616C=
ENST00000644022.1:n.658C=
ENST00000644708.1:n.658C=
ENST00000644911.1:n.658C=
ENST00000645266.1:c.252C=	ENSP00000493734.1:p.Asn84=
ENST00000645518.1:c.252C=	ENSP00000493986.1:p.Asn84=
ENST00000646106.1:c.252C=	ENSP00000496437.1:p.Asn84=
ENST00000646505.1:c.252C=	ENSP00000496673.1:p.Asn84=
ENST00000647492.1:c.252C=	ENSP00000495340.1:p.Asn84=
ENST00000276110.6:n.637C=
ENST00000374188.7:c.-465C=	ENSP00000363303.3:n.-465C=
ENST00000374202.6:c.252C=	ENSP00000363318.2:p.Asn84=
ENST00000456850.6:c.24+511C=	ENSP00000388967.2:n.24+511C=
ENST00000464642.5:c.120C=	ENSP00000425233.1:p.Asn40=
ENST00000473378.1:c.189C=	ENSP00000423601.1:p.Asn63=
ENST00000487883.1:c.216C=	ENSP00000423966.1:p.Asn72=
ENST00000512747.3:n.319C=
NM_000206.2:c.252C= , LRG_150t1:c.252C=	NP_000197.1:p.Asn84=
NM_000206.3:c.252C= MANE Select	NP_000197.1:p.Asn84=