Canonical Allele Identifier: CA359428097

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35867481T>A (hg19) ; chr5:g.35867379T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867379T>A , CM000667.2:g.35867379T>A	GRCh38
NC_000005.9:g.35867481T>A , CM000667.1:g.35867481T>A	GRCh37
NC_000005.8:g.35903238T>A	NCBI36
NG_009567.1:g.15491T>A , LRG_74:g.15491T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.295T>A MANE Select	ENSP00000306157.3:p.Phe99Ile
ENST00000303115.7:c.295T>A	ENSP00000306157.3:p.Phe99Ile
ENST00000506850.5:c.295T>A	ENSP00000421207.1:p.Phe99Ile
ENST00000511031.1:n.429T>A
ENST00000511982.1:c.295T>A	ENSP00000425309.1:p.Phe99Ile
ENST00000514217.5:c.295T>A	ENSP00000427688.1:p.Phe99Ile
NM_002185.3:c.295T>A	NP_002176.2:p.Phe99Ile
NR_120485.1:n.398T>A
XM_005248299.2:c.295T>A	XP_005248356.1:p.Phe99Ile
XM_005248300.1:c.295T>A	XP_005248357.1:p.Phe99Ile
XM_011514037.1:c.295T>A	XP_011512339.1:p.Phe99Ile
NM_002185.4:c.295T>A	NP_002176.2:p.Phe99Ile
NR_120485.2:n.424T>A
XM_005248299.4:c.295T>A	XP_005248356.1:p.Phe99Ile
NM_002185.5:c.295T>A MANE Select	NP_002176.2:p.Phe99Ile
NR_120485.3:n.382T>A