Canonical Allele Identifier: CA1075040794
Gene: IL7R HGNC NCBI

Linked Data

dbSNP Id: rs1759956368

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867060_35867061del , CM000667.2:g.35867060_35867061del GRCh38
NC_000005.9:g.35867162_35867163del , CM000667.1:g.35867162_35867163del GRCh37
NC_000005.8:g.35902919_35902920del NCBI36
NG_009567.1:g.15172_15173del , LRG_74:g.15172_15173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.222-246_222-245del MANE Select ENSP00000306157.3:n.222-246_222-245del
ENST00000303115.7:c.222-246_222-245del ENSP00000306157.3:n.222-246_222-245del
ENST00000506850.5:c.222-246_222-245del ENSP00000421207.1:n.222-246_222-245del
ENST00000511031.1:n.356-246_356-245del
ENST00000511982.1:c.222-246_222-245del ENSP00000425309.1:n.222-246_222-245del
ENST00000514217.5:c.222-246_222-245del ENSP00000427688.1:n.222-246_222-245del
NM_002185.3:c.222-246_222-245del NP_002176.2:n.222-246_222-245del
NR_120485.1:n.325-246_325-245del
XM_005248299.2:c.222-246_222-245del XP_005248356.1:n.222-246_222-245del
XM_005248300.1:c.222-246_222-245del XP_005248357.1:n.222-246_222-245del
XM_011514037.1:c.222-246_222-245del XP_011512339.1:n.222-246_222-245del
NM_002185.4:c.222-246_222-245del NP_002176.2:n.222-246_222-245del
NR_120485.2:n.351-246_351-245del
XM_005248299.4:c.222-246_222-245del XP_005248356.1:n.222-246_222-245del
NM_002185.5:c.222-246_222-245del MANE Select NP_002176.2:n.222-246_222-245del
NR_120485.3:n.309-246_309-245del