Canonical Allele Identifier: CA2708535253

Gene: IL7R

Linked Data

• dbSNP Id: rs2149899376

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867624del , CM000667.2:g.35867624del	GRCh38
NC_000005.9:g.35867726del , CM000667.1:g.35867726del	GRCh37
NC_000005.8:g.35903483del	NCBI36
NG_009567.1:g.15736del , LRG_74:g.15736del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+161del MANE Select	ENSP00000306157.3:n.379+161del
ENST00000303115.7:c.379+161del	ENSP00000306157.3:n.379+161del
ENST00000506850.5:c.379+161del	ENSP00000421207.1:n.379+161del
ENST00000514217.5:c.379+161del	ENSP00000427688.1:n.379+161del
NM_002185.3:c.379+161del	NP_002176.2:n.379+161del
NR_120485.1:n.482+161del
XM_005248299.2:c.379+161del	XP_005248356.1:n.379+161del
XM_005248300.1:c.379+161del	XP_005248357.1:n.379+161del
XM_011514037.1:c.379+161del	XP_011512339.1:n.379+161del
NM_002185.4:c.379+161del	NP_002176.2:n.379+161del
NR_120485.2:n.508+161del
XM_005248299.4:c.379+161del	XP_005248356.1:n.379+161del
NM_002185.5:c.379+161del MANE Select	NP_002176.2:n.379+161del
NR_120485.3:n.466+161del