Canonical Allele Identifier: CA2673534957

Gene: IL7R

Linked Data

• gnomAD v4: 5-35867530-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867532_35867533del , CM000667.2:g.35867532_35867533del	GRCh38
NC_000005.9:g.35867634_35867635del , CM000667.1:g.35867634_35867635del	GRCh37
NC_000005.8:g.35903391_35903392del	NCBI36
NG_009567.1:g.15644_15645del , LRG_74:g.15644_15645del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+69_379+70del MANE Select	ENSP00000306157.3:n.379+69_379+70del
ENST00000303115.7:c.379+69_379+70del	ENSP00000306157.3:n.379+69_379+70del
ENST00000506850.5:c.379+69_379+70del	ENSP00000421207.1:n.379+69_379+70del
ENST00000511982.1:c.448_449del	ENSP00000425309.1:p.Leu150ValfsTer3
ENST00000514217.5:c.379+69_379+70del	ENSP00000427688.1:n.379+69_379+70del
NM_002185.3:c.379+69_379+70del	NP_002176.2:n.379+69_379+70del
NR_120485.1:n.482+69_482+70del
XM_005248299.2:c.379+69_379+70del	XP_005248356.1:n.379+69_379+70del
XM_005248300.1:c.379+69_379+70del	XP_005248357.1:n.379+69_379+70del
XM_011514037.1:c.379+69_379+70del	XP_011512339.1:n.379+69_379+70del
NM_002185.4:c.379+69_379+70del	NP_002176.2:n.379+69_379+70del
NR_120485.2:n.508+69_508+70del
XM_005248299.4:c.379+69_379+70del	XP_005248356.1:n.379+69_379+70del
NM_002185.5:c.379+69_379+70del MANE Select	NP_002176.2:n.379+69_379+70del
NR_120485.3:n.466+69_466+70del