Canonical Allele Identifier: CA2695202701
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35873612_35873619del , CM000667.2:g.35873612_35873619del GRCh38
NC_000005.9:g.35873714_35873721del , CM000667.1:g.35873714_35873721del GRCh37
NC_000005.8:g.35909471_35909478del NCBI36
NG_009567.1:g.21724_21731del , LRG_74:g.21724_21731del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.670_677del MANE Select ENSP00000306157.3:p.Tyr224GlnfsTer7
ENST00000303115.7:c.670_677del ENSP00000306157.3:p.Tyr224GlnfsTer7
ENST00000505093.1:c.79_86del ENSP00000426069.1:p.Tyr27GlnfsTer7
ENST00000506850.5:c.670_677del ENSP00000421207.1:p.Tyr224GlnfsTer7
ENST00000509668.1:n.412_419del
ENST00000514217.5:c.538-1900_538-1893del ENSP00000427688.1:n.538-1900_538-1893del
NM_002185.3:c.670_677del NP_002176.2:p.Tyr224GlnfsTer7
NR_120485.1:n.641-1900_641-1893del
XM_005248299.2:c.670_677del XP_005248356.1:p.Tyr224GlnfsTer7
XM_005248300.1:c.670_677del XP_005248357.1:p.Tyr224GlnfsTer7
XM_011514037.1:c.670_677del XP_011512339.1:p.Tyr224GlnfsTer7
NM_002185.4:c.670_677del NP_002176.2:p.Tyr224GlnfsTer7
NR_120485.2:n.667-1900_667-1893del
XM_005248299.4:c.670_677del XP_005248356.1:p.Tyr224GlnfsTer7
NM_002185.5:c.670_677del MANE Select NP_002176.2:p.Tyr224GlnfsTer7
NR_120485.3:n.625-1900_625-1893del