Canonical Allele Identifier: CA877807577

Gene: IL2RG

Linked Data

• dbSNP Id: rs1242360622
• gnomAD v3: X-71109494-TTC-T
• gnomAD v4: X-71109494-TTC-T
• MyVariant Identifiers: chrX:g.70329345_70329346del (hg19) ; chrX:g.71109495_71109496del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71109501_71109502del , CM000685.2:g.71109501_71109502del	GRCh38
NC_000023.10:g.70329351_70329352del , CM000685.1:g.70329351_70329352del	GRCh37
NC_000023.9:g.70246076_70246077del	NCBI36
NG_009088.1:g.7058_7059del , LRG_150:g.7058_7059del
NG_021141.1:g.2293_2294del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.595-106_595-105del	ENSP00000421262.2:n.595-106_595-105del
ENST00000696903.1:n.646-106_646-105del
ENST00000374202.7:c.595-106_595-105del MANE Select	ENSP00000363318.3:n.595-106_595-105del
ENST00000642473.1:n.959-106_959-105del
ENST00000644022.1:n.861-106_861-105del
ENST00000644708.1:n.1001-106_1001-105del
ENST00000644911.1:n.1001-106_1001-105del
ENST00000645266.1:c.595-106_595-105del	ENSP00000493734.1:n.595-106_595-105del
ENST00000645518.1:c.595-106_595-105del	ENSP00000493986.1:n.595-106_595-105del
ENST00000646106.1:c.595-106_595-105del	ENSP00000496437.1:n.595-106_595-105del
ENST00000646505.1:c.595-106_595-105del	ENSP00000496673.1:n.595-106_595-105del
ENST00000647492.1:c.595-106_595-105del	ENSP00000495340.1:n.595-106_595-105del
ENST00000276110.6:n.1188-106_1188-105del
ENST00000374188.7:c.-122-106_-122-105del	ENSP00000363303.3:n.-122-106_-122-105del
ENST00000374202.6:c.595-106_595-105del	ENSP00000363318.2:n.595-106_595-105del
ENST00000456850.6:c.25-106_25-105del	ENSP00000388967.2:n.25-106_25-105del
ENST00000464642.5:c.463-106_463-105del	ENSP00000425233.1:n.463-106_463-105del
ENST00000482750.5:c.8-106_8-105del
ENST00000512747.3:n.522-106_522-105del
NM_000206.2:c.595-106_595-105del , LRG_150t1:c.595-106_595-105del	NP_000197.1:n.595-106_595-105del
NM_000206.3:c.595-106_595-105del MANE Select	NP_000197.1:n.595-106_595-105del