Canonical Allele Identifier: CA1539045924
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867374A= , CM000667.2:g.35867374A= GRCh38
NC_000005.9:g.35867476A= , CM000667.1:g.35867476A= GRCh37
NC_000005.8:g.35903233A= NCBI36
NG_009567.1:g.15486A= , LRG_74:g.15486A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.290A= MANE Select ENSP00000306157.3:p.Lys97=
ENST00000303115.7:c.290A= ENSP00000306157.3:p.Lys97=
ENST00000506850.5:c.290A= ENSP00000421207.1:p.Lys97=
ENST00000511031.1:n.424A=
ENST00000511982.1:c.290A= ENSP00000425309.1:p.Lys97=
ENST00000514217.5:c.290A= ENSP00000427688.1:p.Lys97=
NM_002185.3:c.290A= NP_002176.2:p.Lys97=
NR_120485.1:n.393A=
XM_005248299.2:c.290A= XP_005248356.1:p.Lys97=
XM_005248300.1:c.290A= XP_005248357.1:p.Lys97=
XM_011514037.1:c.290A= XP_011512339.1:p.Lys97=
NM_002185.4:c.290A= NP_002176.2:p.Lys97=
NR_120485.2:n.419A=
XM_005248299.4:c.290A= XP_005248356.1:p.Lys97=
NM_002185.5:c.290A= MANE Select NP_002176.2:p.Lys97=
NR_120485.3:n.377A=