Canonical Allele Identifier: CA1539046064

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867421_35867423delinsGAA , CM000667.2:g.35867421_35867423delinsGAA	GRCh38
NC_000005.9:g.35867523_35867525delinsGAA , CM000667.1:g.35867523_35867525delinsGAA	GRCh37
NC_000005.8:g.35903280_35903282delinsGAA	NCBI36
NG_009567.1:g.15533_15535delinsGAA , LRG_74:g.15533_15535delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.337_339delinsGAA MANE Select	ENSP00000306157.3:p.Glu113=
ENST00000303115.7:c.337_339delinsGAA	ENSP00000306157.3:p.Glu113=
ENST00000506850.5:c.337_339delinsGAA	ENSP00000421207.1:p.Glu113=
ENST00000511031.1:n.471_473delinsGAA
ENST00000511982.1:c.337_339delinsGAA	ENSP00000425309.1:p.Glu113=
ENST00000514217.5:c.337_339delinsGAA	ENSP00000427688.1:p.Glu113=
NM_002185.3:c.337_339delinsGAA	NP_002176.2:p.Glu113=
NR_120485.1:n.440_442delinsGAA
XM_005248299.2:c.337_339delinsGAA	XP_005248356.1:p.Glu113=
XM_005248300.1:c.337_339delinsGAA	XP_005248357.1:p.Glu113=
XM_011514037.1:c.337_339delinsGAA	XP_011512339.1:p.Glu113=
NM_002185.4:c.337_339delinsGAA	NP_002176.2:p.Glu113=
NR_120485.2:n.466_468delinsGAA
XM_005248299.4:c.337_339delinsGAA	XP_005248356.1:p.Glu113=
NM_002185.5:c.337_339delinsGAA MANE Select	NP_002176.2:p.Glu113=
NR_120485.3:n.424_426delinsGAA