Canonical Allele Identifier: CA1539046271

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867491T= , CM000667.2:g.35867491T=	GRCh38
NC_000005.9:g.35867593T= , CM000667.1:g.35867593T=	GRCh37
NC_000005.8:g.35903350T=	NCBI36
NG_009567.1:g.15603T= , LRG_74:g.15603T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.379+28T= MANE Select	ENSP00000306157.3:n.379+28T=
ENST00000303115.7:c.379+28T=	ENSP00000306157.3:n.379+28T=
ENST00000506850.5:c.379+28T=	ENSP00000421207.1:n.379+28T=
ENST00000511982.1:c.407T=	ENSP00000425309.1:p.Leu136=
ENST00000514217.5:c.379+28T=	ENSP00000427688.1:n.379+28T=
NM_002185.3:c.379+28T=	NP_002176.2:n.379+28T=
NR_120485.1:n.482+28T=
XM_005248299.2:c.379+28T=	XP_005248356.1:n.379+28T=
XM_005248300.1:c.379+28T=	XP_005248357.1:n.379+28T=
XM_011514037.1:c.379+28T=	XP_011512339.1:n.379+28T=
NM_002185.4:c.379+28T=	NP_002176.2:n.379+28T=
NR_120485.2:n.508+28T=
XM_005248299.4:c.379+28T=	XP_005248356.1:n.379+28T=
NM_002185.5:c.379+28T= MANE Select	NP_002176.2:n.379+28T=
NR_120485.3:n.466+28T=