Canonical Allele Identifier: CA1539046054

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867419G= , CM000667.2:g.35867419G=	GRCh38
NC_000005.9:g.35867521G= , CM000667.1:g.35867521G=	GRCh37
NC_000005.8:g.35903278G=	NCBI36
NG_009567.1:g.15531G= , LRG_74:g.15531G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.335G= MANE Select	ENSP00000306157.3:p.Gly112=
ENST00000303115.7:c.335G=	ENSP00000306157.3:p.Gly112=
ENST00000506850.5:c.335G=	ENSP00000421207.1:p.Gly112=
ENST00000511031.1:n.469G=
ENST00000511982.1:c.335G=	ENSP00000425309.1:p.Gly112=
ENST00000514217.5:c.335G=	ENSP00000427688.1:p.Gly112=
NM_002185.3:c.335G=	NP_002176.2:p.Gly112=
NR_120485.1:n.438G=
XM_005248299.2:c.335G=	XP_005248356.1:p.Gly112=
XM_005248300.1:c.335G=	XP_005248357.1:p.Gly112=
XM_011514037.1:c.335G=	XP_011512339.1:p.Gly112=
NM_002185.4:c.335G=	NP_002176.2:p.Gly112=
NR_120485.2:n.464G=
XM_005248299.4:c.335G=	XP_005248356.1:p.Gly112=
NM_002185.5:c.335G= MANE Select	NP_002176.2:p.Gly112=
NR_120485.3:n.422G=