Canonical Allele Identifier: CA2199177414

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707788_98707789delinsCG , CM000677.2:g.98707788_98707789delinsCG	GRCh38
NC_000015.9:g.99251017_99251018delinsCG , CM000677.1:g.99251017_99251018delinsCG	GRCh37
NC_000015.8:g.97068540_97068541delinsCG	NCBI36
NG_009492.1:g.63257_63258delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000649865.1:c.321_322delinsCG	ENSP00000496919.1:p.Arg107=
ENST00000650285.1:c.321_322delinsCG MANE Select	ENSP00000497069.1:p.Arg107=
ENST00000268035.10:c.321_322delinsCG	ENSP00000268035.6:p.Arg107=
ENST00000558762.5:c.321_322delinsCG	ENSP00000453007.1:p.Arg107=
ENST00000559925.5:n.321_322delinsCG
NM_000875.4:c.321_322delinsCG	NP_000866.1:p.Arg107=
NM_001291858.1:c.321_322delinsCG	NP_001278787.1:p.Arg107=
XM_011521513.1:c.321_322delinsCG	XP_011519815.1:p.Arg107=
XM_011521514.1:c.321_322delinsCG	XP_011519816.1:p.Arg107=
XM_011521515.1:c.321_322delinsCG	XP_011519817.1:p.Arg107=
XM_017022136.1:c.396_397delinsCG	XP_016877625.1:p.Arg132=
XM_017022137.1:c.396_397delinsCG	XP_016877626.1:p.Arg132=
XM_017022138.1:c.396_397delinsCG	XP_016877627.1:p.Arg132=
XM_017022139.1:c.-43_-42delinsCG	XP_016877628.1:n.-43_-42delinsCG
NM_000875.5:c.321_322delinsCG MANE Select	NP_000866.1:p.Arg107=
NM_001291858.2:c.321_322delinsCG	NP_001278787.1:p.Arg107=