Canonical Allele Identifier: CA359430582

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35873604A>T (hg19) ; chr5:g.35873502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873502A>T , CM000667.2:g.35873502A>T	GRCh38
NC_000005.9:g.35873604A>T , CM000667.1:g.35873604A>T	GRCh37
NC_000005.8:g.35909361A>T	NCBI36
NG_009567.1:g.21614A>T , LRG_74:g.21614A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.560A>T MANE Select	ENSP00000306157.3:p.Lys187Met
ENST00000303115.7:c.560A>T	ENSP00000306157.3:p.Lys187Met
ENST00000506850.5:c.560A>T	ENSP00000421207.1:p.Lys187Met
ENST00000509668.1:n.302A>T
ENST00000514217.5:c.538-2010A>T	ENSP00000427688.1:n.538-2010A>T
NM_002185.3:c.560A>T	NP_002176.2:p.Lys187Met
NR_120485.1:n.641-2010A>T
XM_005248299.2:c.560A>T	XP_005248356.1:p.Lys187Met
XM_005248300.1:c.560A>T	XP_005248357.1:p.Lys187Met
XM_011514037.1:c.560A>T	XP_011512339.1:p.Lys187Met
NM_002185.4:c.560A>T	NP_002176.2:p.Lys187Met
NR_120485.2:n.667-2010A>T
XM_005248299.4:c.560A>T	XP_005248356.1:p.Lys187Met
NM_002185.5:c.560A>T MANE Select	NP_002176.2:p.Lys187Met
NR_120485.3:n.625-2010A>T