Canonical Allele Identifier: CA1539046265

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867488G= , CM000667.2:g.35867488G=	GRCh38
NC_000005.9:g.35867590G= , CM000667.1:g.35867590G=	GRCh37
NC_000005.8:g.35903347G=	NCBI36
NG_009567.1:g.15600G= , LRG_74:g.15600G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+25G= MANE Select	ENSP00000306157.3:n.379+25G=
ENST00000303115.7:c.379+25G=	ENSP00000306157.3:n.379+25G=
ENST00000506850.5:c.379+25G=	ENSP00000421207.1:n.379+25G=
ENST00000511982.1:c.404G=	ENSP00000425309.1:p.Trp135=
ENST00000514217.5:c.379+25G=	ENSP00000427688.1:n.379+25G=
NM_002185.3:c.379+25G=	NP_002176.2:n.379+25G=
NR_120485.1:n.482+25G=
XM_005248299.2:c.379+25G=	XP_005248356.1:n.379+25G=
XM_005248300.1:c.379+25G=	XP_005248357.1:n.379+25G=
XM_011514037.1:c.379+25G=	XP_011512339.1:n.379+25G=
NM_002185.4:c.379+25G=	NP_002176.2:n.379+25G=
NR_120485.2:n.508+25G=
XM_005248299.4:c.379+25G=	XP_005248356.1:n.379+25G=
NM_002185.5:c.379+25G= MANE Select	NP_002176.2:n.379+25G=
NR_120485.3:n.466+25G=