Canonical Allele Identifier: CA413496809

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70330481T>G (hg19) ; chrX:g.71110631T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110631T>G , CM000685.2:g.71110631T>G	GRCh38
NC_000023.10:g.70330481T>G , CM000685.1:g.70330481T>G	GRCh37
NC_000023.9:g.70247206T>G	NCBI36
NG_009088.1:g.5923A>C , LRG_150:g.5923A>C
NG_021141.1:g.1158A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.327A>C	ENSP00000421262.2:p.Glu109Asp
ENST00000696903.1:n.378A>C
ENST00000374202.7:c.327A>C MANE Select	ENSP00000363318.3:p.Glu109Asp
ENST00000642473.1:n.691A>C
ENST00000644022.1:n.733A>C
ENST00000644708.1:n.733A>C
ENST00000644911.1:n.733A>C
ENST00000645266.1:c.327A>C	ENSP00000493734.1:p.Glu109Asp
ENST00000645518.1:c.327A>C	ENSP00000493986.1:p.Glu109Asp
ENST00000646106.1:c.327A>C	ENSP00000496437.1:p.Glu109Asp
ENST00000646505.1:c.327A>C	ENSP00000496673.1:p.Glu109Asp
ENST00000647492.1:c.327A>C	ENSP00000495340.1:p.Glu109Asp
ENST00000276110.6:n.712A>C
ENST00000374188.7:c.-390A>C	ENSP00000363303.3:n.-390A>C
ENST00000374202.6:c.327A>C	ENSP00000363318.2:p.Glu109Asp
ENST00000456850.6:c.24+794A>C	ENSP00000388967.2:n.24+794A>C
ENST00000464642.5:c.195A>C	ENSP00000425233.1:p.Glu65Asp
ENST00000473378.1:c.264A>C	ENSP00000423601.1:p.Glu88Asp
ENST00000487883.1:c.291A>C	ENSP00000423966.1:p.Glu97Asp
ENST00000512747.3:n.394A>C
NM_000206.2:c.327A>C , LRG_150t1:c.327A>C	NP_000197.1:p.Glu109Asp
NM_000206.3:c.327A>C MANE Select	NP_000197.1:p.Glu109Asp