Canonical Allele Identifier: CA2821726298
Gene: IL2RG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71109512_71109513insAGG , CM000685.2:g.71109512_71109513insAGG GRCh38
NC_000023.10:g.70329362_70329363insAGG , CM000685.1:g.70329362_70329363insAGG GRCh37
NC_000023.9:g.70246087_70246088insAGG NCBI36
NG_009088.1:g.7041_7042insCCT , LRG_150:g.7041_7042insCCT
NG_021141.1:g.2276_2277insCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.595-123_595-122insCCT ENSP00000421262.2:n.595-123_595-122insCCT
ENST00000696903.1:n.646-123_646-122insCCT
ENST00000374202.7:c.595-123_595-122insCCT MANE Select ENSP00000363318.3:n.595-123_595-122insCCT
ENST00000642473.1:n.959-123_959-122insCCT
ENST00000644022.1:n.861-123_861-122insCCT
ENST00000644708.1:n.1001-123_1001-122insCCT
ENST00000644911.1:n.1001-123_1001-122insCCT
ENST00000645266.1:c.595-123_595-122insCCT ENSP00000493734.1:n.595-123_595-122insCCT
ENST00000645518.1:c.595-123_595-122insCCT ENSP00000493986.1:n.595-123_595-122insCCT
ENST00000646106.1:c.595-123_595-122insCCT ENSP00000496437.1:n.595-123_595-122insCCT
ENST00000646505.1:c.595-123_595-122insCCT ENSP00000496673.1:n.595-123_595-122insCCT
ENST00000647492.1:c.595-123_595-122insCCT ENSP00000495340.1:n.595-123_595-122insCCT
ENST00000276110.6:n.1188-123_1188-122insCCT
ENST00000374188.7:c.-122-123_-122-122insCCT ENSP00000363303.3:n.-122-123_-122-122insCCT
ENST00000374202.6:c.595-123_595-122insCCT ENSP00000363318.2:n.595-123_595-122insCCT
ENST00000456850.6:c.25-123_25-122insCCT ENSP00000388967.2:n.25-123_25-122insCCT
ENST00000464642.5:c.463-123_463-122insCCT ENSP00000425233.1:n.463-123_463-122insCCT
ENST00000482750.5:c.8-123_8-122insCCT
ENST00000512747.3:n.522-123_522-122insCCT
NM_000206.2:c.595-123_595-122insCCT , LRG_150t1:c.595-123_595-122insCCT NP_000197.1:n.595-123_595-122insCCT
NM_000206.3:c.595-123_595-122insCCT MANE Select NP_000197.1:n.595-123_595-122insCCT