Canonical Allele Identifier: CA2199282049

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908853A= , CM000677.2:g.98908853A=	GRCh38
NC_000015.9:g.99452082A= , CM000677.1:g.99452082A=	GRCh37
NC_000015.8:g.97269605A=	NCBI36
NG_009492.1:g.264322A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1416A=	ENSP00000496919.1:p.Gln472=
ENST00000650285.1:c.1416A= MANE Select	ENSP00000497069.1:p.Gln472=
ENST00000268035.10:c.1416A=	ENSP00000268035.6:p.Gln472=
ENST00000558762.5:c.1416A=	ENSP00000453007.1:p.Gln472=
ENST00000558898.1:c.507A=	ENSP00000454115.1:p.Gln169=
ENST00000559582.1:n.323A=
ENST00000559925.5:n.1416A=
NM_000875.4:c.1416A=	NP_000866.1:p.Gln472=
NM_001291858.1:c.1416A=	NP_001278787.1:p.Gln472=
XM_011521513.1:c.1479A=	XP_011519815.1:p.Gln493=
XM_011521514.1:c.1479A=	XP_011519816.1:p.Gln493=
XM_011521515.1:c.1479A=	XP_011519817.1:p.Gln493=
XM_011521516.1:c.507A=	XP_011519818.1:p.Gln169=
XM_011521517.1:c.81A=	XP_011519819.1:p.Gln27=
XM_011521516.2:c.507A=	XP_011519818.1:p.Gln169=
XM_011521517.2:c.81A=	XP_011519819.1:p.Gln27=
XM_017022136.1:c.1491A=	XP_016877625.1:p.Gln497=
XM_017022137.1:c.1491A=	XP_016877626.1:p.Gln497=
XM_017022138.1:c.1491A=	XP_016877627.1:p.Gln497=
XM_017022139.1:c.1053A=	XP_016877628.1:p.Gln351=
XM_024449913.1:c.507A=	XP_024305681.1:p.Gln169=
NM_000875.5:c.1416A= MANE Select	NP_000866.1:p.Gln472=
NM_001291858.2:c.1416A=	NP_001278787.1:p.Gln472=