Canonical Allele Identifier: CA2199177437

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707798C= , CM000677.2:g.98707798C=	GRCh38
NC_000015.9:g.99251027C= , CM000677.1:g.99251027C=	GRCh37
NC_000015.8:g.97068550C=	NCBI36
NG_009492.1:g.63267C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649865.1:c.331C=	ENSP00000496919.1:p.Leu111=
ENST00000650285.1:c.331C= MANE Select	ENSP00000497069.1:p.Leu111=
ENST00000268035.10:c.331C=	ENSP00000268035.6:p.Leu111=
ENST00000558762.5:c.331C=	ENSP00000453007.1:p.Leu111=
ENST00000559925.5:n.331C=
NM_000875.4:c.331C=	NP_000866.1:p.Leu111=
NM_001291858.1:c.331C=	NP_001278787.1:p.Leu111=
XM_011521513.1:c.331C=	XP_011519815.1:p.Leu111=
XM_011521514.1:c.331C=	XP_011519816.1:p.Leu111=
XM_011521515.1:c.331C=	XP_011519817.1:p.Leu111=
XM_017022136.1:c.406C=	XP_016877625.1:p.Leu136=
XM_017022137.1:c.406C=	XP_016877626.1:p.Leu136=
XM_017022138.1:c.406C=	XP_016877627.1:p.Leu136=
XM_017022139.1:c.-33C=	XP_016877628.1:n.-33C=
NM_000875.5:c.331C= MANE Select	NP_000866.1:p.Leu111=
NM_001291858.2:c.331C=	NP_001278787.1:p.Leu111=