Canonical Allele Identifier: CA359430575

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35873601C>A (hg19) ; chr5:g.35873499C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873499C>A , CM000667.2:g.35873499C>A	GRCh38
NC_000005.9:g.35873601C>A , CM000667.1:g.35873601C>A	GRCh37
NC_000005.8:g.35909358C>A	NCBI36
NG_009567.1:g.21611C>A , LRG_74:g.21611C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.557C>A MANE Select	ENSP00000306157.3:p.Thr186Lys
ENST00000303115.7:c.557C>A	ENSP00000306157.3:p.Thr186Lys
ENST00000506850.5:c.557C>A	ENSP00000421207.1:p.Thr186Lys
ENST00000509668.1:n.299C>A
ENST00000514217.5:c.538-2013C>A	ENSP00000427688.1:n.538-2013C>A
NM_002185.3:c.557C>A	NP_002176.2:p.Thr186Lys
NR_120485.1:n.641-2013C>A
XM_005248299.2:c.557C>A	XP_005248356.1:p.Thr186Lys
XM_005248300.1:c.557C>A	XP_005248357.1:p.Thr186Lys
XM_011514037.1:c.557C>A	XP_011512339.1:p.Thr186Lys
NM_002185.4:c.557C>A	NP_002176.2:p.Thr186Lys
NR_120485.2:n.667-2013C>A
XM_005248299.4:c.557C>A	XP_005248356.1:p.Thr186Lys
NM_002185.5:c.557C>A MANE Select	NP_002176.2:p.Thr186Lys
NR_120485.3:n.625-2013C>A