Canonical Allele Identifier: CA2199258364

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98886233G= , CM000677.2:g.98886233G=	GRCh38
NC_000015.9:g.99429462G= , CM000677.1:g.99429462G=	GRCh37
NC_000015.8:g.97246985G=	NCBI36
NG_009492.1:g.241702G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000875.5:c.641-5092G= MANE Select	NP_000866.1:n.641-5092G=
ENST00000650285.1:c.641-5092G= MANE Select	ENSP00000497069.1:n.641-5092G=
NM_000875.4:c.641-5092G=	NP_000866.1:n.641-5092G=
NM_001291858.1:c.641-5092G=	NP_001278787.1:n.641-5092G=
NM_001291858.2:c.641-5092G=	NP_001278787.1:n.641-5092G=
ENST00000268035.10:c.641-5092G=	ENSP00000268035.6:n.641-5092G=
ENST00000557873.5:n.138-5092G=
ENST00000557938.5:n.43-5092G=
ENST00000558355.1:c.278-5092G=	ENSP00000453630.1:n.278-5092G=
ENST00000558762.5:c.641-5092G=	ENSP00000453007.1:n.641-5092G=
ENST00000559925.5:n.641-5092G=
ENST00000560186.5:n.76-5092G=
ENST00000560277.5:n.121-5092G=
ENST00000649865.1:c.641-5092G=	ENSP00000496919.1:n.641-5092G=
XM_011521513.1:c.704-5092G=	XP_011519815.1:n.704-5092G=
XM_011521514.1:c.704-5092G=	XP_011519816.1:n.704-5092G=
XM_011521515.1:c.704-5092G=	XP_011519817.1:n.704-5092G=
XM_017022136.1:c.716-5092G=	XP_016877625.1:n.716-5092G=
XM_017022137.1:c.716-5092G=	XP_016877626.1:n.716-5092G=
XM_017022138.1:c.716-5092G=	XP_016877627.1:n.716-5092G=
XM_017022139.1:c.278-5092G=	XP_016877628.1:n.278-5092G=