Canonical Allele Identifier: CA1539065810

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35857751C= , CM000667.2:g.35857751C=	GRCh38
NC_000005.9:g.35857853C= , CM000667.1:g.35857853C=	GRCh37
NC_000005.8:g.35893610C=	NCBI36
NG_009567.1:g.5863C= , LRG_74:g.5863C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.82+692C= MANE Select	ENSP00000306157.3:n.82+692C=
ENST00000303115.7:c.82+692C=	ENSP00000306157.3:n.82+692C=
ENST00000506850.5:c.82+692C=	ENSP00000421207.1:n.82+692C=
ENST00000508941.5:c.82+692C=	ENSP00000426426.1:n.82+692C=
ENST00000511031.1:n.217-3101C=
ENST00000511982.1:c.82+692C=	ENSP00000425309.1:n.82+692C=
ENST00000514217.5:c.82+692C=	ENSP00000427688.1:n.82+692C=
ENST00000515665.1:c.82+692C=	ENSP00000425538.1:n.82+692C=
NM_002185.3:c.82+692C=	NP_002176.2:n.82+692C=
NR_120485.1:n.185+692C=
XM_005248299.2:c.82+692C=	XP_005248356.1:n.82+692C=
XM_005248300.1:c.82+692C=	XP_005248357.1:n.82+692C=
XM_011514037.1:c.82+692C=	XP_011512339.1:n.82+692C=
NM_002185.4:c.82+692C=	NP_002176.2:n.82+692C=
NR_120485.2:n.211+692C=
XM_005248299.4:c.82+692C=	XP_005248356.1:n.82+692C=
XR_001742635.1:n.1533+1116G=
NM_002185.5:c.82+692C= MANE Select	NP_002176.2:n.82+692C=
NR_120485.3:n.169+692C=