Canonical Allele Identifier: CA2765881627

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867110_35867111del , CM000667.2:g.35867110_35867111del	GRCh38
NC_000005.9:g.35867212_35867213del , CM000667.1:g.35867212_35867213del	GRCh37
NC_000005.8:g.35902969_35902970del	NCBI36
NG_009567.1:g.15222_15223del , LRG_74:g.15222_15223del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.222-196_222-195del MANE Select	ENSP00000306157.3:n.222-196_222-195del
ENST00000303115.7:c.222-196_222-195del	ENSP00000306157.3:n.222-196_222-195del
ENST00000506850.5:c.222-196_222-195del	ENSP00000421207.1:n.222-196_222-195del
ENST00000511031.1:n.356-196_356-195del
ENST00000511982.1:c.222-196_222-195del	ENSP00000425309.1:n.222-196_222-195del
ENST00000514217.5:c.222-196_222-195del	ENSP00000427688.1:n.222-196_222-195del
NM_002185.3:c.222-196_222-195del	NP_002176.2:n.222-196_222-195del
NR_120485.1:n.325-196_325-195del
XM_005248299.2:c.222-196_222-195del	XP_005248356.1:n.222-196_222-195del
XM_005248300.1:c.222-196_222-195del	XP_005248357.1:n.222-196_222-195del
XM_011514037.1:c.222-196_222-195del	XP_011512339.1:n.222-196_222-195del
NM_002185.4:c.222-196_222-195del	NP_002176.2:n.222-196_222-195del
NR_120485.2:n.351-196_351-195del
XM_005248299.4:c.222-196_222-195del	XP_005248356.1:n.222-196_222-195del
NM_002185.5:c.222-196_222-195del MANE Select	NP_002176.2:n.222-196_222-195del
NR_120485.3:n.309-196_309-195del