Canonical Allele Identifier: CA413497027

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70330778G>C (hg19) ; chrX:g.71110928G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110928G>C , CM000685.2:g.71110928G>C	GRCh38
NC_000023.10:g.70330778G>C , CM000685.1:g.70330778G>C	GRCh37
NC_000023.9:g.70247503G>C	NCBI36
NG_009088.1:g.5626C>G , LRG_150:g.5626C>G
NG_021141.1:g.861C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.238C>G	ENSP00000421262.2:p.Pro80Ala
ENST00000696903.1:n.289C>G
ENST00000374202.7:c.238C>G MANE Select	ENSP00000363318.3:p.Pro80Ala
ENST00000642473.1:n.602C>G
ENST00000644022.1:n.644C>G
ENST00000644708.1:n.644C>G
ENST00000644911.1:n.644C>G
ENST00000645266.1:c.238C>G	ENSP00000493734.1:p.Pro80Ala
ENST00000645518.1:c.238C>G	ENSP00000493986.1:p.Pro80Ala
ENST00000646106.1:c.238C>G	ENSP00000496437.1:p.Pro80Ala
ENST00000646505.1:c.238C>G	ENSP00000496673.1:p.Pro80Ala
ENST00000647492.1:c.238C>G	ENSP00000495340.1:p.Pro80Ala
ENST00000276110.6:n.623C>G
ENST00000374188.7:c.-479C>G	ENSP00000363303.3:n.-479C>G
ENST00000374202.6:c.238C>G	ENSP00000363318.2:p.Pro80Ala
ENST00000456850.6:c.24+497C>G	ENSP00000388967.2:n.24+497C>G
ENST00000464642.5:c.106C>G	ENSP00000425233.1:p.Pro36Ala
ENST00000473378.1:c.175C>G	ENSP00000423601.1:p.Pro59Ala
ENST00000487883.1:c.202C>G	ENSP00000423966.1:p.Pro68Ala
ENST00000512747.3:n.305C>G
NM_000206.2:c.238C>G , LRG_150t1:c.238C>G	NP_000197.1:p.Pro80Ala
NM_000206.3:c.238C>G MANE Select	NP_000197.1:p.Pro80Ala