Canonical Allele Identifier: CA2694023088
Gene: IL2RG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71110788_71110791del , CM000685.2:g.71110788_71110791del GRCh38
NC_000023.10:g.70330638_70330641del , CM000685.1:g.70330638_70330641del GRCh37
NC_000023.9:g.70247363_70247366del NCBI36
NG_009088.1:g.5765_5768del , LRG_150:g.5765_5768del
NG_021141.1:g.1000_1003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.270-101_270-98del ENSP00000421262.2:n.270-101_270-98del
ENST00000696903.1:n.321-101_321-98del
ENST00000374202.7:c.270-101_270-98del MANE Select ENSP00000363318.3:n.270-101_270-98del
ENST00000642473.1:n.634-101_634-98del
ENST00000644022.1:n.676-101_676-98del
ENST00000644708.1:n.676-101_676-98del
ENST00000644911.1:n.676-101_676-98del
ENST00000645266.1:c.270-101_270-98del ENSP00000493734.1:n.270-101_270-98del
ENST00000645518.1:c.270-101_270-98del ENSP00000493986.1:n.270-101_270-98del
ENST00000646106.1:c.270-101_270-98del ENSP00000496437.1:n.270-101_270-98del
ENST00000646505.1:c.270-101_270-98del ENSP00000496673.1:n.270-101_270-98del
ENST00000647492.1:c.270-101_270-98del ENSP00000495340.1:n.270-101_270-98del
ENST00000276110.6:n.655-101_655-98del
ENST00000374188.7:c.-447-101_-447-98del ENSP00000363303.3:n.-447-101_-447-98del
ENST00000374202.6:c.270-101_270-98del ENSP00000363318.2:n.270-101_270-98del
ENST00000456850.6:c.24+636_24+639del ENSP00000388967.2:n.24+636_24+639del
ENST00000464642.5:c.138-101_138-98del ENSP00000425233.1:n.138-101_138-98del
ENST00000473378.1:c.207-101_207-98del ENSP00000423601.1:n.207-101_207-98del
ENST00000487883.1:c.234-101_234-98del ENSP00000423966.1:n.234-101_234-98del
ENST00000512747.3:n.337-101_337-98del
NM_000206.2:c.270-101_270-98del , LRG_150t1:c.270-101_270-98del NP_000197.1:n.270-101_270-98del
NM_000206.3:c.270-101_270-98del MANE Select NP_000197.1:n.270-101_270-98del