Canonical Allele Identifier: CA1539065824
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35857762A= , CM000667.2:g.35857762A= GRCh38
NC_000005.9:g.35857864A= , CM000667.1:g.35857864A= GRCh37
NC_000005.8:g.35893621A= NCBI36
NG_009567.1:g.5874A= , LRG_74:g.5874A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.82+703A= MANE Select ENSP00000306157.3:n.82+703A=
ENST00000303115.7:c.82+703A= ENSP00000306157.3:n.82+703A=
ENST00000506850.5:c.82+703A= ENSP00000421207.1:n.82+703A=
ENST00000508941.5:c.82+703A= ENSP00000426426.1:n.82+703A=
ENST00000511031.1:n.217-3090A=
ENST00000511982.1:c.82+703A= ENSP00000425309.1:n.82+703A=
ENST00000514217.5:c.82+703A= ENSP00000427688.1:n.82+703A=
ENST00000515665.1:c.82+703A= ENSP00000425538.1:n.82+703A=
NM_002185.3:c.82+703A= NP_002176.2:n.82+703A=
NR_120485.1:n.185+703A=
XM_005248299.2:c.82+703A= XP_005248356.1:n.82+703A=
XM_005248300.1:c.82+703A= XP_005248357.1:n.82+703A=
XM_011514037.1:c.82+703A= XP_011512339.1:n.82+703A=
NM_002185.4:c.82+703A= NP_002176.2:n.82+703A=
NR_120485.2:n.211+703A=
XM_005248299.4:c.82+703A= XP_005248356.1:n.82+703A=
XR_001742635.1:n.1533+1105T=
NM_002185.5:c.82+703A= MANE Select NP_002176.2:n.82+703A=
NR_120485.3:n.169+703A=