Canonical Allele Identifier: CA2199282034

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908840C= , CM000677.2:g.98908840C=	GRCh38
NC_000015.9:g.99452069C= , CM000677.1:g.99452069C=	GRCh37
NC_000015.8:g.97269592C=	NCBI36
NG_009492.1:g.264309C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1403C=	ENSP00000496919.1:p.Thr468=
ENST00000650285.1:c.1403C= MANE Select	ENSP00000497069.1:p.Thr468=
ENST00000268035.10:c.1403C=	ENSP00000268035.6:p.Thr468=
ENST00000558762.5:c.1403C=	ENSP00000453007.1:p.Thr468=
ENST00000558898.1:c.494C=	ENSP00000454115.1:p.Thr165=
ENST00000559582.1:n.310C=
ENST00000559925.5:n.1403C=
NM_000875.4:c.1403C=	NP_000866.1:p.Thr468=
NM_001291858.1:c.1403C=	NP_001278787.1:p.Thr468=
XM_011521513.1:c.1466C=	XP_011519815.1:p.Thr489=
XM_011521514.1:c.1466C=	XP_011519816.1:p.Thr489=
XM_011521515.1:c.1466C=	XP_011519817.1:p.Thr489=
XM_011521516.1:c.494C=	XP_011519818.1:p.Thr165=
XM_011521517.1:c.68C=	XP_011519819.1:p.Thr23=
XM_011521516.2:c.494C=	XP_011519818.1:p.Thr165=
XM_011521517.2:c.68C=	XP_011519819.1:p.Thr23=
XM_017022136.1:c.1478C=	XP_016877625.1:p.Thr493=
XM_017022137.1:c.1478C=	XP_016877626.1:p.Thr493=
XM_017022138.1:c.1478C=	XP_016877627.1:p.Thr493=
XM_017022139.1:c.1040C=	XP_016877628.1:p.Thr347=
XM_024449913.1:c.494C=	XP_024305681.1:p.Thr165=
NM_000875.5:c.1403C= MANE Select	NP_000866.1:p.Thr468=
NM_001291858.2:c.1403C=	NP_001278787.1:p.Thr468=