Canonical Allele Identifier: CA1539046126
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867437G= , CM000667.2:g.35867437G= GRCh38
NC_000005.9:g.35867539G= , CM000667.1:g.35867539G= GRCh37
NC_000005.8:g.35903296G= NCBI36
NG_009567.1:g.15549G= , LRG_74:g.15549G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.353G= MANE Select ENSP00000306157.3:p.Cys118=
ENST00000303115.7:c.353G= ENSP00000306157.3:p.Cys118=
ENST00000506850.5:c.353G= ENSP00000421207.1:p.Cys118=
ENST00000511031.1:n.487G=
ENST00000511982.1:c.353G= ENSP00000425309.1:p.Cys118=
ENST00000514217.5:c.353G= ENSP00000427688.1:p.Cys118=
NM_002185.3:c.353G= NP_002176.2:p.Cys118=
NR_120485.1:n.456G=
XM_005248299.2:c.353G= XP_005248356.1:p.Cys118=
XM_005248300.1:c.353G= XP_005248357.1:p.Cys118=
XM_011514037.1:c.353G= XP_011512339.1:p.Cys118=
NM_002185.4:c.353G= NP_002176.2:p.Cys118=
NR_120485.2:n.482G=
XM_005248299.4:c.353G= XP_005248356.1:p.Cys118=
NM_002185.5:c.353G= MANE Select NP_002176.2:p.Cys118=
NR_120485.3:n.440G=