Canonical Allele Identifier: CA7751943

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98891599G>A , CM000677.2:g.98891599G>A	GRCh38
NC_000015.9:g.99434828G>A , CM000677.1:g.99434828G>A	GRCh37
NC_000015.8:g.97252351G>A	NCBI36
NG_009492.1:g.247068G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.915G>A	ENSP00000496919.1:p.Gln305=
ENST00000650285.1:c.915G>A MANE Select	ENSP00000497069.1:p.Gln305=
ENST00000268035.10:c.915G>A	ENSP00000268035.6:p.Gln305=
ENST00000557873.5:n.412G>A
ENST00000557938.5:n.317G>A
ENST00000558355.1:c.552G>A	ENSP00000453630.1:p.Gln184=
ENST00000558762.5:c.915G>A	ENSP00000453007.1:p.Gln305=
ENST00000558898.1:c.6G>A	ENSP00000454115.1:p.Gln2=
ENST00000559925.5:n.915G>A
ENST00000560186.5:n.350G>A
ENST00000560277.5:n.395G>A
ENST00000560432.1:n.489G>A
NM_000875.4:c.915G>A	NP_000866.1:p.Gln305=
NM_001291858.1:c.915G>A	NP_001278787.1:p.Gln305=
XM_011521513.1:c.978G>A	XP_011519815.1:p.Gln326=
XM_011521514.1:c.978G>A	XP_011519816.1:p.Gln326=
XM_011521515.1:c.978G>A	XP_011519817.1:p.Gln326=
XM_011521516.1:c.6G>A	XP_011519818.1:p.Gln2=
XM_011521516.2:c.6G>A	XP_011519818.1:p.Gln2=
XM_017022136.1:c.990G>A	XP_016877625.1:p.Gln330=
XM_017022137.1:c.990G>A	XP_016877626.1:p.Gln330=
XM_017022138.1:c.990G>A	XP_016877627.1:p.Gln330=
XM_017022139.1:c.552G>A	XP_016877628.1:p.Gln184=
XM_024449913.1:c.6G>A	XP_024305681.1:p.Gln2=
NM_000875.5:c.915G>A MANE Select	NP_000866.1:p.Gln305=
NM_001291858.2:c.915G>A	NP_001278787.1:p.Gln305=