Canonical Allele Identifier: CA202287822
Gene: IL2RA HGNC NCBI

Linked Data

dbSNP Id: rs932937510
gnomAD v3: 10-6011289-AT-A
gnomAD v4: 10-6011289-AT-A
MyVariant Identifiers: chr10:g.6053253del (hg19) chr10:g.6011290del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6011296del , CM000672.2:g.6011296del GRCh38
NC_000010.10:g.6053259del , CM000672.1:g.6053259del GRCh37
NC_000010.9:g.6093265del NCBI36
NG_007403.1:g.56020del , LRG_73:g.56020del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379959.8:c.*1582del MANE Select ENSP00000369293.3:n.*1582del
ENST00000649218.1:n.2216del
ENST00000379959.7:c.*1582del ENSP00000369293.3:n.*1582del
NM_000417.2:c.*1582del , LRG_73t1:c.*1582del NP_000408.1:n.*1582del
NM_001308242.1:c.*1582del NP_001295171.1:n.*1582del
NM_001308243.1:c.*1582del NP_001295172.1:n.*1582del
NM_000417.3:c.*1582del MANE Select NP_000408.1:n.*1582del
NM_001308242.2:c.*1582del NP_001295171.1:n.*1582del
NM_001308243.2:c.*1582del NP_001295172.1:n.*1582del
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