Canonical Allele Identifier: CA2501319562

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867264_35867267del , CM000667.2:g.35867264_35867267del	GRCh38
NC_000005.9:g.35867366_35867369del , CM000667.1:g.35867366_35867369del	GRCh37
NC_000005.8:g.35903123_35903126del	NCBI36
NG_009567.1:g.15376_15379del , LRG_74:g.15376_15379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.222-42_222-39del MANE Select	ENSP00000306157.3:n.222-42_222-39del
ENST00000303115.7:c.222-42_222-39del	ENSP00000306157.3:n.222-42_222-39del
ENST00000506850.5:c.222-42_222-39del	ENSP00000421207.1:n.222-42_222-39del
ENST00000511031.1:n.356-42_356-39del
ENST00000511982.1:c.222-42_222-39del	ENSP00000425309.1:n.222-42_222-39del
ENST00000514217.5:c.222-42_222-39del	ENSP00000427688.1:n.222-42_222-39del
NM_002185.3:c.222-42_222-39del	NP_002176.2:n.222-42_222-39del
NR_120485.1:n.325-42_325-39del
XM_005248299.2:c.222-42_222-39del	XP_005248356.1:n.222-42_222-39del
XM_005248300.1:c.222-42_222-39del	XP_005248357.1:n.222-42_222-39del
XM_011514037.1:c.222-42_222-39del	XP_011512339.1:n.222-42_222-39del
NM_002185.4:c.222-42_222-39del	NP_002176.2:n.222-42_222-39del
NR_120485.2:n.351-42_351-39del
XM_005248299.4:c.222-42_222-39del	XP_005248356.1:n.222-42_222-39del
NM_002185.5:c.222-42_222-39del MANE Select	NP_002176.2:n.222-42_222-39del
NR_120485.3:n.309-42_309-39del