Canonical Allele Identifier: CA2199286815

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98956205T= , CM000677.2:g.98956205T=	GRCh38
NC_000015.9:g.99499434T= , CM000677.1:g.99499434T=	GRCh37
NC_000015.8:g.97316957T=	NCBI36
NG_009492.1:g.311674T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3720-856T=	ENSP00000496919.1:n.3720-856T=
ENST00000650285.1:c.3723-856T= MANE Select	ENSP00000497069.1:n.3723-856T=
ENST00000268035.10:c.3723-856T=	ENSP00000268035.6:n.3723-856T=
ENST00000558751.1:n.317-856T=
ENST00000558762.5:c.3720-856T=	ENSP00000453007.1:n.3720-856T=
NM_000875.4:c.3723-856T=	NP_000866.1:n.3723-856T=
NM_001291858.1:c.3720-856T=	NP_001278787.1:n.3720-856T=
XM_011521513.1:c.3786-856T=	XP_011519815.1:n.3786-856T=
XM_011521514.1:c.3786-856T=	XP_011519816.1:n.3786-856T=
XM_011521515.1:c.3783-856T=	XP_011519817.1:n.3783-856T=
XM_011521516.1:c.2814-856T=	XP_011519818.1:n.2814-856T=
XM_011521517.1:c.2388-856T=	XP_011519819.1:n.2388-856T=
XM_011521516.2:c.2814-856T=	XP_011519818.1:n.2814-856T=
XM_011521517.2:c.2388-856T=	XP_011519819.1:n.2388-856T=
XM_017022136.1:c.3798-856T=	XP_016877625.1:n.3798-856T=
XM_017022137.1:c.3798-856T=	XP_016877626.1:n.3798-856T=
XM_017022138.1:c.3795-856T=	XP_016877627.1:n.3795-856T=
XM_017022139.1:c.3360-856T=	XP_016877628.1:n.3360-856T=
XM_024449913.1:c.2814-856T=	XP_024305681.1:n.2814-856T=
NM_000875.5:c.3723-856T= MANE Select	NP_000866.1:n.3723-856T=
NM_001291858.2:c.3720-856T=	NP_001278787.1:n.3720-856T=