Canonical Allele Identifier: CA1539052435

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873559G= , CM000667.2:g.35873559G=	GRCh38
NC_000005.9:g.35873661G= , CM000667.1:g.35873661G=	GRCh37
NC_000005.8:g.35909418G=	NCBI36
NG_009567.1:g.21671G= , LRG_74:g.21671G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.617G= MANE Select	ENSP00000306157.3:p.Arg206=
ENST00000303115.7:c.617G=	ENSP00000306157.3:p.Arg206=
ENST00000505093.1:c.26G=	ENSP00000426069.1:p.Arg9=
ENST00000506850.5:c.617G=	ENSP00000421207.1:p.Arg206=
ENST00000509668.1:n.359G=
ENST00000514217.5:c.538-1953G=	ENSP00000427688.1:n.538-1953G=
NM_002185.3:c.617G=	NP_002176.2:p.Arg206=
NR_120485.1:n.641-1953G=
XM_005248299.2:c.617G=	XP_005248356.1:p.Arg206=
XM_005248300.1:c.617G=	XP_005248357.1:p.Arg206=
XM_011514037.1:c.617G=	XP_011512339.1:p.Arg206=
NM_002185.4:c.617G=	NP_002176.2:p.Arg206=
NR_120485.2:n.667-1953G=
XM_005248299.4:c.617G=	XP_005248356.1:p.Arg206=
NM_002185.5:c.617G= MANE Select	NP_002176.2:p.Arg206=
NR_120485.3:n.625-1953G=