Canonical Allele Identifier: CA2673534946
Gene: IL7R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867344_35867351del , CM000667.2:g.35867344_35867351del GRCh38
NC_000005.9:g.35867446_35867453del , CM000667.1:g.35867446_35867453del GRCh37
NC_000005.8:g.35903203_35903210del NCBI36
NG_009567.1:g.15456_15463del , LRG_74:g.15456_15463del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.260_267del MANE Select ENSP00000306157.3:p.Lys87ArgfsTer?
ENST00000303115.7:c.260_267del ENSP00000306157.3:p.Lys87ArgfsTer?
ENST00000506850.5:c.260_267del ENSP00000421207.1:p.Lys87ArgfsTer?
ENST00000511031.1:n.394_401del
ENST00000511982.1:c.260_267del ENSP00000425309.1:p.Lys87ArgfsTer?
ENST00000514217.5:c.260_267del ENSP00000427688.1:p.Lys87ArgfsTer?
NM_002185.3:c.260_267del NP_002176.2:p.Lys87ArgfsTer?
NR_120485.1:n.363_370del
XM_005248299.2:c.260_267del XP_005248356.1:p.Lys87ArgfsTer?
XM_005248300.1:c.260_267del XP_005248357.1:p.Lys87ArgfsTer?
XM_011514037.1:c.260_267del XP_011512339.1:p.Lys87ArgfsTer?
NM_002185.4:c.260_267del NP_002176.2:p.Lys87ArgfsTer?
NR_120485.2:n.389_396del
XM_005248299.4:c.260_267del XP_005248356.1:p.Lys87ArgfsTer?
NM_002185.5:c.260_267del MANE Select NP_002176.2:p.Lys87ArgfsTer?
NR_120485.3:n.347_354del