Canonical Allele Identifier: CA330970455
Gene: IL2RG HGNC NCBI

Linked Data

dbSNP Id: rs193921149

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71110947del , CM000685.2:g.71110947del GRCh38
NC_000023.10:g.70330797del , CM000685.1:g.70330797del GRCh37
NC_000023.9:g.70247522del NCBI36
NG_009088.1:g.5608del , LRG_150:g.5608del
NG_021141.1:g.843del

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.220del ENSP00000421262.2:p.Trp74GlyfsTer?
ENST00000696903.1:n.271del
ENST00000374202.7:c.220del MANE Select ENSP00000363318.3:p.Trp74GlyfsTer?
ENST00000642473.1:n.584del
ENST00000644022.1:n.626del
ENST00000644708.1:n.626del
ENST00000644911.1:n.626del
ENST00000645266.1:c.220del ENSP00000493734.1:p.Trp74GlyfsTer?
ENST00000645518.1:c.220del ENSP00000493986.1:p.Trp74GlyfsTer?
ENST00000646106.1:c.220del ENSP00000496437.1:p.Trp74GlyfsTer?
ENST00000646505.1:c.220del ENSP00000496673.1:p.Trp74GlyfsTer?
ENST00000647492.1:c.220del ENSP00000495340.1:p.Trp74GlyfsTer?
ENST00000276110.6:n.605del
ENST00000374188.7:c.-497del ENSP00000363303.3:n.-497del
ENST00000374202.6:c.220del ENSP00000363318.2:p.Trp74GlyfsTer?
ENST00000456850.6:c.24+479del ENSP00000388967.2:n.24+479del
ENST00000464642.5:c.88del ENSP00000425233.1:p.Trp30GlyfsTer?
ENST00000473378.1:c.157del ENSP00000423601.1:p.Trp53GlyfsTer?
ENST00000487883.1:c.184del ENSP00000423966.1:p.Trp62GlyfsTer?
ENST00000512747.3:n.287del
NM_000206.2:c.220del , LRG_150t1:c.220del NP_000197.1:p.Trp74GlyfsTer?
NM_000206.3:c.220del MANE Select NP_000197.1:p.Trp74GlyfsTer?