Canonical Allele Identifier: CA413495895

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70329118T>G (hg19) ; chrX:g.71109268T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.717A>C	ENSP00000421262.2:p.Glu239Asp
ENST00000696903.1:n.768A>C
ENST00000374202.7:c.717A>C MANE Select	ENSP00000363318.3:p.Glu239Asp
ENST00000642473.1:n.1081A>C
ENST00000644022.1:n.983A>C
ENST00000644708.1:n.1123A>C
ENST00000644911.1:n.1123A>C
ENST00000645266.1:c.717A>C	ENSP00000493734.1:p.Glu239Asp
ENST00000645518.1:c.717A>C	ENSP00000493986.1:p.Glu239Asp
ENST00000646106.1:c.717A>C	ENSP00000496437.1:p.Glu239Asp
ENST00000646505.1:c.717A>C	ENSP00000496673.1:p.Glu239Asp
ENST00000647492.1:c.717A>C	ENSP00000495340.1:p.Glu239Asp
ENST00000276110.6:n.1310A>C
ENST00000374188.7:c.1A>C	ENSP00000363303.3:p.Met1Leu
ENST00000374202.6:c.717A>C	ENSP00000363318.2:p.Glu239Asp
ENST00000456850.6:c.147A>C	ENSP00000388967.2:p.Glu49Asp
ENST00000464642.5:c.585A>C	ENSP00000425233.1:p.Glu195Asp
ENST00000482750.5:c.130A>C
ENST00000512747.3:n.644A>C
NM_000206.2:c.717A>C , LRG_150t1:c.717A>C	NP_000197.1:p.Glu239Asp
NM_000206.3:c.717A>C MANE Select	NP_000197.1:p.Glu239Asp