Canonical Allele Identifier: CA667039918

Gene: IL2RA

Linked Data

• dbSNP Id: rs1183198482
• gnomAD v3: 10-6011019-CTGTT-C
• gnomAD v4: 10-6011019-CTGTT-C
• MyVariant Identifiers: chr10:g.6052983_6052986del (hg19) ; chr10:g.6011020_6011023del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6011023_6011026del , CM000672.2:g.6011023_6011026del	GRCh38
NC_000010.10:g.6052986_6052989del , CM000672.1:g.6052986_6052989del	GRCh37
NC_000010.9:g.6092992_6092995del	NCBI36
NG_007403.1:g.56287_56290del , LRG_73:g.56287_56290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379959.8:c.*1849_*1852del MANE Select	ENSP00000369293.3:n.*1849_*1852del
ENST00000649218.1:n.2483_2486del
ENST00000379959.7:c.*1849_*1852del	ENSP00000369293.3:n.*1849_*1852del
NM_000417.2:c.*1849_*1852del , LRG_73t1:c.*1849_*1852del	NP_000408.1:n.*1849_*1852del
NM_001308242.1:c.*1849_*1852del	NP_001295171.1:n.*1849_*1852del
NM_001308243.1:c.*1849_*1852del	NP_001295172.1:n.*1849_*1852del
NM_000417.3:c.*1849_*1852del MANE Select	NP_000408.1:n.*1849_*1852del
NM_001308242.2:c.*1849_*1852del	NP_001295171.1:n.*1849_*1852del
NM_001308243.2:c.*1849_*1852del	NP_001295172.1:n.*1849_*1852del