Canonical Allele Identifier: CA1539055097

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35875125G= , CM000667.2:g.35875125G=	GRCh38
NC_000005.9:g.35875227G= , CM000667.1:g.35875227G=	GRCh37
NC_000005.8:g.35910984G=	NCBI36
NG_009567.1:g.23237G= , LRG_74:g.23237G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.801-387G= MANE Select	ENSP00000306157.3:n.801-387G=
ENST00000303115.7:c.801-387G=	ENSP00000306157.3:n.801-387G=
ENST00000505093.1:c.116-387G=	ENSP00000426069.1:n.116-387G=
ENST00000506850.5:c.707-387G=	ENSP00000421207.1:n.707-387G=
ENST00000509668.1:n.543-387G=
ENST00000514217.5:c.538-387G=	ENSP00000427688.1:n.538-387G=
NM_002185.3:c.801-387G=	NP_002176.2:n.801-387G=
NR_120485.1:n.641-387G=
XM_005248299.2:c.707-387G=	XP_005248356.1:n.707-387G=
XM_005248300.1:c.707-387G=	XP_005248357.1:n.707-387G=
XM_011514037.1:c.800-385G=	XP_011512339.1:n.800-385G=
NM_002185.4:c.801-387G=	NP_002176.2:n.801-387G=
NR_120485.2:n.667-387G=
XM_005248299.4:c.707-387G=	XP_005248356.1:n.707-387G=
NM_002185.5:c.801-387G= MANE Select	NP_002176.2:n.801-387G=
NR_120485.3:n.625-387G=