Canonical Allele Identifier: CA1539052274
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35873503_35873504delinsGC , CM000667.2:g.35873503_35873504delinsGC GRCh38
NC_000005.9:g.35873605_35873606delinsGC , CM000667.1:g.35873605_35873606delinsGC GRCh37
NC_000005.8:g.35909362_35909363delinsGC NCBI36
NG_009567.1:g.21615_21616delinsGC , LRG_74:g.21615_21616delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.561_562delinsGC MANE Select ENSP00000306157.3:p.Lys187=
ENST00000303115.7:c.561_562delinsGC ENSP00000306157.3:p.Lys187=
ENST00000506850.5:c.561_562delinsGC ENSP00000421207.1:p.Lys187=
ENST00000509668.1:n.303_304delinsGC
ENST00000514217.5:c.538-2009_538-2008delinsGC ENSP00000427688.1:n.538-2009_538-2008deli...
NM_002185.3:c.561_562delinsGC NP_002176.2:p.Lys187=
NR_120485.1:n.641-2009_641-2008delinsGC
XM_005248299.2:c.561_562delinsGC XP_005248356.1:p.Lys187=
XM_005248300.1:c.561_562delinsGC XP_005248357.1:p.Lys187=
XM_011514037.1:c.561_562delinsGC XP_011512339.1:p.Lys187=
NM_002185.4:c.561_562delinsGC NP_002176.2:p.Lys187=
NR_120485.2:n.667-2009_667-2008delinsGC
XM_005248299.4:c.561_562delinsGC XP_005248356.1:p.Lys187=
NM_002185.5:c.561_562delinsGC MANE Select NP_002176.2:p.Lys187=
NR_120485.3:n.625-2009_625-2008delinsGC