Canonical Allele Identifier: CA1539052590

Gene: IL7R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873616A= , CM000667.2:g.35873616A=	GRCh38
NC_000005.9:g.35873718A= , CM000667.1:g.35873718A=	GRCh37
NC_000005.8:g.35909475A=	NCBI36
NG_009567.1:g.21728A= , LRG_74:g.21728A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.674A= MANE Select	ENSP00000306157.3:p.Tyr225=
ENST00000303115.7:c.674A=	ENSP00000306157.3:p.Tyr225=
ENST00000505093.1:c.83A=	ENSP00000426069.1:p.Tyr28=
ENST00000506850.5:c.674A=	ENSP00000421207.1:p.Tyr225=
ENST00000509668.1:n.416A=
ENST00000514217.5:c.538-1896A=	ENSP00000427688.1:n.538-1896A=
NM_002185.3:c.674A=	NP_002176.2:p.Tyr225=
NR_120485.1:n.641-1896A=
XM_005248299.2:c.674A=	XP_005248356.1:p.Tyr225=
XM_005248300.1:c.674A=	XP_005248357.1:p.Tyr225=
XM_011514037.1:c.674A=	XP_011512339.1:p.Tyr225=
NM_002185.4:c.674A=	NP_002176.2:p.Tyr225=
NR_120485.2:n.667-1896A=
XM_005248299.4:c.674A=	XP_005248356.1:p.Tyr225=
NM_002185.5:c.674A= MANE Select	NP_002176.2:p.Tyr225=
NR_120485.3:n.625-1896A=