Canonical Allele Identifier: CA1539065826

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35857764A= , CM000667.2:g.35857764A=	GRCh38
NC_000005.9:g.35857866A= , CM000667.1:g.35857866A=	GRCh37
NC_000005.8:g.35893623A=	NCBI36
NG_009567.1:g.5876A= , LRG_74:g.5876A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.82+705A= MANE Select	ENSP00000306157.3:n.82+705A=
ENST00000303115.7:c.82+705A=	ENSP00000306157.3:n.82+705A=
ENST00000506850.5:c.82+705A=	ENSP00000421207.1:n.82+705A=
ENST00000508941.5:c.82+705A=	ENSP00000426426.1:n.82+705A=
ENST00000511031.1:n.217-3088A=
ENST00000511982.1:c.82+705A=	ENSP00000425309.1:n.82+705A=
ENST00000514217.5:c.82+705A=	ENSP00000427688.1:n.82+705A=
ENST00000515665.1:c.82+705A=	ENSP00000425538.1:n.82+705A=
NM_002185.3:c.82+705A=	NP_002176.2:n.82+705A=
NR_120485.1:n.185+705A=
XM_005248299.2:c.82+705A=	XP_005248356.1:n.82+705A=
XM_005248300.1:c.82+705A=	XP_005248357.1:n.82+705A=
XM_011514037.1:c.82+705A=	XP_011512339.1:n.82+705A=
NM_002185.4:c.82+705A=	NP_002176.2:n.82+705A=
NR_120485.2:n.211+705A=
XM_005248299.4:c.82+705A=	XP_005248356.1:n.82+705A=
XR_001742635.1:n.1533+1103T=
NM_002185.5:c.82+705A= MANE Select	NP_002176.2:n.82+705A=
NR_120485.3:n.169+705A=