Canonical Allele Identifier: CA1539046257

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867484G= , CM000667.2:g.35867484G=	GRCh38
NC_000005.9:g.35867586G= , CM000667.1:g.35867586G=	GRCh37
NC_000005.8:g.35903343G=	NCBI36
NG_009567.1:g.15596G= , LRG_74:g.15596G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+21G= MANE Select	ENSP00000306157.3:n.379+21G=
ENST00000303115.7:c.379+21G=	ENSP00000306157.3:n.379+21G=
ENST00000506850.5:c.379+21G=	ENSP00000421207.1:n.379+21G=
ENST00000511982.1:c.400G=	ENSP00000425309.1:p.Val134=
ENST00000514217.5:c.379+21G=	ENSP00000427688.1:n.379+21G=
NM_002185.3:c.379+21G=	NP_002176.2:n.379+21G=
NR_120485.1:n.482+21G=
XM_005248299.2:c.379+21G=	XP_005248356.1:n.379+21G=
XM_005248300.1:c.379+21G=	XP_005248357.1:n.379+21G=
XM_011514037.1:c.379+21G=	XP_011512339.1:n.379+21G=
NM_002185.4:c.379+21G=	NP_002176.2:n.379+21G=
NR_120485.2:n.508+21G=
XM_005248299.4:c.379+21G=	XP_005248356.1:n.379+21G=
NM_002185.5:c.379+21G= MANE Select	NP_002176.2:n.379+21G=
NR_120485.3:n.466+21G=