Canonical Allele Identifier: CA1539055666

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35875491A= , CM000667.2:g.35875491A=	GRCh38
NC_000005.9:g.35875593A= , CM000667.1:g.35875593A=	GRCh37
NC_000005.8:g.35911350A=	NCBI36
NG_009567.1:g.23603A= , LRG_74:g.23603A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002185.5:c.801-21A= MANE Select	NP_002176.2:n.801-21A=
ENST00000303115.8:c.801-21A= MANE Select	ENSP00000306157.3:n.801-21A=
NM_002185.3:c.801-21A=	NP_002176.2:n.801-21A=
NM_002185.4:c.801-21A=	NP_002176.2:n.801-21A=
NR_120485.1:n.641-21A=
NR_120485.2:n.667-21A=
NR_120485.3:n.625-21A=
ENST00000303115.7:c.801-21A=	ENSP00000306157.3:n.801-21A=
ENST00000505093.1:c.116-21A=	ENSP00000426069.1:n.116-21A=
ENST00000505875.1:n.78A=
ENST00000506850.5:c.707-21A=	ENSP00000421207.1:n.707-21A=
ENST00000509668.1:n.543-21A=
ENST00000514217.5:c.538-21A=	ENSP00000427688.1:n.538-21A=
XM_005248299.2:c.707-21A=	XP_005248356.1:n.707-21A=
XM_005248299.4:c.707-21A=	XP_005248356.1:n.707-21A=
XM_005248300.1:c.707-21A=	XP_005248357.1:n.707-21A=
XM_011514037.1:c.800-19A=	XP_011512339.1:n.800-19A=