Canonical Allele Identifier: CA1539048949

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35871088G= , CM000667.2:g.35871088G=	GRCh38
NC_000005.9:g.35871190G= , CM000667.1:g.35871190G=	GRCh37
NC_000005.8:g.35906947G=	NCBI36
NG_009567.1:g.19200G= , LRG_74:g.19200G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002185.5:c.412G= MANE Select	NP_002176.2:p.Val138=
ENST00000303115.8:c.412G= MANE Select	ENSP00000306157.3:p.Val138=
NM_002185.3:c.412G=	NP_002176.2:p.Val138=
NM_002185.4:c.412G=	NP_002176.2:p.Val138=
NR_120485.1:n.515G=
NR_120485.2:n.541G=
NR_120485.3:n.499G=
ENST00000303115.7:c.412G=	ENSP00000306157.3:p.Val138=
ENST00000506850.5:c.412G=	ENSP00000421207.1:p.Val138=
ENST00000514217.5:c.412G=	ENSP00000427688.1:p.Val138=
XM_005248299.2:c.412G=	XP_005248356.1:p.Val138=
XM_005248299.4:c.412G=	XP_005248356.1:p.Val138=
XM_005248300.1:c.412G=	XP_005248357.1:p.Val138=
XM_011514037.1:c.412G=	XP_011512339.1:p.Val138=