Canonical Allele Identifier: CA1539052358

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873534G= , CM000667.2:g.35873534G=	GRCh38
NC_000005.9:g.35873636G= , CM000667.1:g.35873636G=	GRCh37
NC_000005.8:g.35909393G=	NCBI36
NG_009567.1:g.21646G= , LRG_74:g.21646G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.592G= MANE Select	ENSP00000306157.3:p.Ala198=
ENST00000303115.7:c.592G=	ENSP00000306157.3:p.Ala198=
ENST00000505093.1:c.1G=	ENSP00000426069.1:p.Ala1=
ENST00000506850.5:c.592G=	ENSP00000421207.1:p.Ala198=
ENST00000509668.1:n.334G=
ENST00000514217.5:c.538-1978G=	ENSP00000427688.1:n.538-1978G=
NM_002185.3:c.592G=	NP_002176.2:p.Ala198=
NR_120485.1:n.641-1978G=
XM_005248299.2:c.592G=	XP_005248356.1:p.Ala198=
XM_005248300.1:c.592G=	XP_005248357.1:p.Ala198=
XM_011514037.1:c.592G=	XP_011512339.1:p.Ala198=
NM_002185.4:c.592G=	NP_002176.2:p.Ala198=
NR_120485.2:n.667-1978G=
XM_005248299.4:c.592G=	XP_005248356.1:p.Ala198=
NM_002185.5:c.592G= MANE Select	NP_002176.2:p.Ala198=
NR_120485.3:n.625-1978G=