Canonical Allele Identifier: CA1539045952

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867385C= , CM000667.2:g.35867385C=	GRCh38
NC_000005.9:g.35867487C= , CM000667.1:g.35867487C=	GRCh37
NC_000005.8:g.35903244C=	NCBI36
NG_009567.1:g.15497C= , LRG_74:g.15497C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.301C= MANE Select	ENSP00000306157.3:p.Leu101=
ENST00000303115.7:c.301C=	ENSP00000306157.3:p.Leu101=
ENST00000506850.5:c.301C=	ENSP00000421207.1:p.Leu101=
ENST00000511031.1:n.435C=
ENST00000511982.1:c.301C=	ENSP00000425309.1:p.Leu101=
ENST00000514217.5:c.301C=	ENSP00000427688.1:p.Leu101=
NM_002185.3:c.301C=	NP_002176.2:p.Leu101=
NR_120485.1:n.404C=
XM_005248299.2:c.301C=	XP_005248356.1:p.Leu101=
XM_005248300.1:c.301C=	XP_005248357.1:p.Leu101=
XM_011514037.1:c.301C=	XP_011512339.1:p.Leu101=
NM_002185.4:c.301C=	NP_002176.2:p.Leu101=
NR_120485.2:n.430C=
XM_005248299.4:c.301C=	XP_005248356.1:p.Leu101=
NM_002185.5:c.301C= MANE Select	NP_002176.2:p.Leu101=
NR_120485.3:n.388C=