Canonical Allele Identifier: CA357950
Gene: IL7R HGNC NCBI

Linked Data

ClinVar Variation Id: 224841
dbSNP Id: rs869312857

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867445dup , CM000667.2:g.35867445dup GRCh38
NC_000005.9:g.35867547dup , CM000667.1:g.35867547dup GRCh37
NC_000005.8:g.35903304dup NCBI36
NG_009567.1:g.15557dup , LRG_74:g.15557dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.361dup MANE Select ENSP00000306157.3:p.Ile121AsnfsTer8
ENST00000303115.7:c.361dup ENSP00000306157.3:p.Ile121AsnfsTer8
ENST00000506850.5:c.361dup ENSP00000421207.1:p.Ile121AsnfsTer8
ENST00000511031.1:n.495dup
ENST00000511982.1:c.361dup ENSP00000425309.1:p.Ile121AsnfsTer8
ENST00000514217.5:c.361dup ENSP00000427688.1:p.Ile121AsnfsTer8
NM_002185.3:c.361dup NP_002176.2:p.Ile121AsnfsTer8
NR_120485.1:n.464dup
XM_005248299.2:c.361dup XP_005248356.1:p.Ile121AsnfsTer8
XM_005248300.1:c.361dup XP_005248357.1:p.Ile121AsnfsTer8
XM_011514037.1:c.361dup XP_011512339.1:p.Ile121AsnfsTer8
NM_002185.4:c.361dup NP_002176.2:p.Ile121AsnfsTer8
NR_120485.2:n.490dup
XM_005248299.4:c.361dup XP_005248356.1:p.Ile121AsnfsTer8
NM_002185.5:c.361dup MANE Select NP_002176.2:p.Ile121AsnfsTer8
NR_120485.3:n.448dup