Canonical Allele Identifier: CA1539046097
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867428G= , CM000667.2:g.35867428G= GRCh38
NC_000005.9:g.35867530G= , CM000667.1:g.35867530G= GRCh37
NC_000005.8:g.35903287G= NCBI36
NG_009567.1:g.15540G= , LRG_74:g.15540G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.344G= MANE Select ENSP00000306157.3:p.Ser115=
ENST00000303115.7:c.344G= ENSP00000306157.3:p.Ser115=
ENST00000506850.5:c.344G= ENSP00000421207.1:p.Ser115=
ENST00000511031.1:n.478G=
ENST00000511982.1:c.344G= ENSP00000425309.1:p.Ser115=
ENST00000514217.5:c.344G= ENSP00000427688.1:p.Ser115=
NM_002185.3:c.344G= NP_002176.2:p.Ser115=
NR_120485.1:n.447G=
XM_005248299.2:c.344G= XP_005248356.1:p.Ser115=
XM_005248300.1:c.344G= XP_005248357.1:p.Ser115=
XM_011514037.1:c.344G= XP_011512339.1:p.Ser115=
NM_002185.4:c.344G= NP_002176.2:p.Ser115=
NR_120485.2:n.473G=
XM_005248299.4:c.344G= XP_005248356.1:p.Ser115=
NM_002185.5:c.344G= MANE Select NP_002176.2:p.Ser115=
NR_120485.3:n.431G=