Canonical Allele Identifier: CA2765881631

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867434_35867438del , CM000667.2:g.35867434_35867438del	GRCh38
NC_000005.9:g.35867536_35867540del , CM000667.1:g.35867536_35867540del	GRCh37
NC_000005.8:g.35903293_35903297del	NCBI36
NG_009567.1:g.15546_15550del , LRG_74:g.15546_15550del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.350_354del MANE Select	ENSP00000306157.3:p.Thr117LysfsTer10
ENST00000303115.7:c.350_354del	ENSP00000306157.3:p.Thr117LysfsTer10
ENST00000506850.5:c.350_354del	ENSP00000421207.1:p.Thr117LysfsTer10
ENST00000511031.1:n.484_488del
ENST00000511982.1:c.350_354del	ENSP00000425309.1:p.Thr117LysfsTer10
ENST00000514217.5:c.350_354del	ENSP00000427688.1:p.Thr117LysfsTer10
NM_002185.3:c.350_354del	NP_002176.2:p.Thr117LysfsTer10
NR_120485.1:n.453_457del
XM_005248299.2:c.350_354del	XP_005248356.1:p.Thr117LysfsTer10
XM_005248300.1:c.350_354del	XP_005248357.1:p.Thr117LysfsTer10
XM_011514037.1:c.350_354del	XP_011512339.1:p.Thr117LysfsTer10
NM_002185.4:c.350_354del	NP_002176.2:p.Thr117LysfsTer10
NR_120485.2:n.479_483del
XM_005248299.4:c.350_354del	XP_005248356.1:p.Thr117LysfsTer10
NM_002185.5:c.350_354del MANE Select	NP_002176.2:p.Thr117LysfsTer10
NR_120485.3:n.437_441del