Canonical Allele Identifier: CA2530973733

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867512_35867513insGT , CM000667.2:g.35867512_35867513insGT	GRCh38
NC_000005.9:g.35867614_35867615insGT , CM000667.1:g.35867614_35867615insGT	GRCh37
NC_000005.8:g.35903371_35903372insGT	NCBI36
NG_009567.1:g.15624_15625insGT , LRG_74:g.15624_15625insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+49_379+50insGT MANE Select	ENSP00000306157.3:n.379+49_379+50insGT
ENST00000303115.7:c.379+49_379+50insGT	ENSP00000306157.3:n.379+49_379+50insGT
ENST00000506850.5:c.379+49_379+50insGT	ENSP00000421207.1:n.379+49_379+50insGT
ENST00000511982.1:c.428_429insGT	ENSP00000425309.1:p.Thr144Ter
ENST00000514217.5:c.379+49_379+50insGT	ENSP00000427688.1:n.379+49_379+50insGT
NM_002185.3:c.379+49_379+50insGT	NP_002176.2:n.379+49_379+50insGT
NR_120485.1:n.482+49_482+50insGT
XM_005248299.2:c.379+49_379+50insGT	XP_005248356.1:n.379+49_379+50insGT
XM_005248300.1:c.379+49_379+50insGT	XP_005248357.1:n.379+49_379+50insGT
XM_011514037.1:c.379+49_379+50insGT	XP_011512339.1:n.379+49_379+50insGT
NM_002185.4:c.379+49_379+50insGT	NP_002176.2:n.379+49_379+50insGT
NR_120485.2:n.508+49_508+50insGT
XM_005248299.4:c.379+49_379+50insGT	XP_005248356.1:n.379+49_379+50insGT
NM_002185.5:c.379+49_379+50insGT MANE Select	NP_002176.2:n.379+49_379+50insGT
NR_120485.3:n.466+49_466+50insGT