Canonical Allele Identifier: CA1539045928

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867379T= , CM000667.2:g.35867379T=	GRCh38
NC_000005.9:g.35867481T= , CM000667.1:g.35867481T=	GRCh37
NC_000005.8:g.35903238T=	NCBI36
NG_009567.1:g.15491T= , LRG_74:g.15491T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.295T= MANE Select	ENSP00000306157.3:p.Phe99=
ENST00000303115.7:c.295T=	ENSP00000306157.3:p.Phe99=
ENST00000506850.5:c.295T=	ENSP00000421207.1:p.Phe99=
ENST00000511031.1:n.429T=
ENST00000511982.1:c.295T=	ENSP00000425309.1:p.Phe99=
ENST00000514217.5:c.295T=	ENSP00000427688.1:p.Phe99=
NM_002185.3:c.295T=	NP_002176.2:p.Phe99=
NR_120485.1:n.398T=
XM_005248299.2:c.295T=	XP_005248356.1:p.Phe99=
XM_005248300.1:c.295T=	XP_005248357.1:p.Phe99=
XM_011514037.1:c.295T=	XP_011512339.1:p.Phe99=
NM_002185.4:c.295T=	NP_002176.2:p.Phe99=
NR_120485.2:n.424T=
XM_005248299.4:c.295T=	XP_005248356.1:p.Phe99=
NM_002185.5:c.295T= MANE Select	NP_002176.2:p.Phe99=
NR_120485.3:n.382T=