Canonical Allele Identifier: CA359427869

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35867449T>G (hg19) ; chr5:g.35867347T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867347T>G , CM000667.2:g.35867347T>G	GRCh38
NC_000005.9:g.35867449T>G , CM000667.1:g.35867449T>G	GRCh37
NC_000005.8:g.35903206T>G	NCBI36
NG_009567.1:g.15459T>G , LRG_74:g.15459T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.263T>G MANE Select	ENSP00000306157.3:p.Leu88Arg
ENST00000303115.7:c.263T>G	ENSP00000306157.3:p.Leu88Arg
ENST00000506850.5:c.263T>G	ENSP00000421207.1:p.Leu88Arg
ENST00000511031.1:n.397T>G
ENST00000511982.1:c.263T>G	ENSP00000425309.1:p.Leu88Arg
ENST00000514217.5:c.263T>G	ENSP00000427688.1:p.Leu88Arg
NM_002185.3:c.263T>G	NP_002176.2:p.Leu88Arg
NR_120485.1:n.366T>G
XM_005248299.2:c.263T>G	XP_005248356.1:p.Leu88Arg
XM_005248300.1:c.263T>G	XP_005248357.1:p.Leu88Arg
XM_011514037.1:c.263T>G	XP_011512339.1:p.Leu88Arg
NM_002185.4:c.263T>G	NP_002176.2:p.Leu88Arg
NR_120485.2:n.392T>G
XM_005248299.4:c.263T>G	XP_005248356.1:p.Leu88Arg
NM_002185.5:c.263T>G MANE Select	NP_002176.2:p.Leu88Arg
NR_120485.3:n.350T>G