Canonical Allele Identifier: CA1539046168

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867447A= , CM000667.2:g.35867447A=	GRCh38
NC_000005.9:g.35867549A= , CM000667.1:g.35867549A=	GRCh37
NC_000005.8:g.35903306A=	NCBI36
NG_009567.1:g.15559A= , LRG_74:g.15559A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.363A= MANE Select	ENSP00000306157.3:p.Ile121=
ENST00000303115.7:c.363A=	ENSP00000306157.3:p.Ile121=
ENST00000506850.5:c.363A=	ENSP00000421207.1:p.Ile121=
ENST00000511031.1:n.497A=
ENST00000511982.1:c.363A=	ENSP00000425309.1:p.Ile121=
ENST00000514217.5:c.363A=	ENSP00000427688.1:p.Ile121=
NM_002185.3:c.363A=	NP_002176.2:p.Ile121=
NR_120485.1:n.466A=
XM_005248299.2:c.363A=	XP_005248356.1:p.Ile121=
XM_005248300.1:c.363A=	XP_005248357.1:p.Ile121=
XM_011514037.1:c.363A=	XP_011512339.1:p.Ile121=
NM_002185.4:c.363A=	NP_002176.2:p.Ile121=
NR_120485.2:n.492A=
XM_005248299.4:c.363A=	XP_005248356.1:p.Ile121=
NM_002185.5:c.363A= MANE Select	NP_002176.2:p.Ile121=
NR_120485.3:n.450A=