Canonical Allele Identifier: CA1539045888

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867351A= , CM000667.2:g.35867351A=	GRCh38
NC_000005.9:g.35867453A= , CM000667.1:g.35867453A=	GRCh37
NC_000005.8:g.35903210A=	NCBI36
NG_009567.1:g.15463A= , LRG_74:g.15463A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.267A= MANE Select	ENSP00000306157.3:p.Gln89=
ENST00000303115.7:c.267A=	ENSP00000306157.3:p.Gln89=
ENST00000506850.5:c.267A=	ENSP00000421207.1:p.Gln89=
ENST00000511031.1:n.401A=
ENST00000511982.1:c.267A=	ENSP00000425309.1:p.Gln89=
ENST00000514217.5:c.267A=	ENSP00000427688.1:p.Gln89=
NM_002185.3:c.267A=	NP_002176.2:p.Gln89=
NR_120485.1:n.370A=
XM_005248299.2:c.267A=	XP_005248356.1:p.Gln89=
XM_005248300.1:c.267A=	XP_005248357.1:p.Gln89=
XM_011514037.1:c.267A=	XP_011512339.1:p.Gln89=
NM_002185.4:c.267A=	NP_002176.2:p.Gln89=
NR_120485.2:n.396A=
XM_005248299.4:c.267A=	XP_005248356.1:p.Gln89=
NM_002185.5:c.267A= MANE Select	NP_002176.2:p.Gln89=
NR_120485.3:n.354A=