Canonical Allele Identifier: CA2608134972

Gene: IL2RA

Linked Data

• gnomAD v4: 10-6011023-T-TTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6011025_6011026insCTG , CM000672.2:g.6011025_6011026insCTG	GRCh38
NC_000010.10:g.6052988_6052989insCTG , CM000672.1:g.6052988_6052989insCTG	GRCh37
NC_000010.9:g.6092994_6092995insCTG	NCBI36
NG_007403.1:g.56286_56287insGCA , LRG_73:g.56286_56287insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379959.8:c.*1848_*1849insGCA MANE Select	ENSP00000369293.3:n.*1848_*1849insGCA
ENST00000649218.1:n.2482_2483insGCA
ENST00000379959.7:c.*1848_*1849insGCA	ENSP00000369293.3:n.*1848_*1849insGCA
NM_000417.2:c.*1848_*1849insGCA , LRG_73t1:c.*1848_*1849insGCA	NP_000408.1:n.*1848_*1849insGCA
NM_001308242.1:c.*1848_*1849insGCA	NP_001295171.1:n.*1848_*1849insGCA
NM_001308243.1:c.*1848_*1849insGCA	NP_001295172.1:n.*1848_*1849insGCA
NM_000417.3:c.*1848_*1849insGCA MANE Select	NP_000408.1:n.*1848_*1849insGCA
NM_001308242.2:c.*1848_*1849insGCA	NP_001295171.1:n.*1848_*1849insGCA
NM_001308243.2:c.*1848_*1849insGCA	NP_001295172.1:n.*1848_*1849insGCA