Canonical Allele Identifier: CA393676097

Gene: IGF1R

Linked Data

• dbSNP Id: rs2151670319
• MyVariant Identifiers: chr15:g.99452066G>A (hg19) ; chr15:g.98908837G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908837G>A , CM000677.2:g.98908837G>A	GRCh38
NC_000015.9:g.99452066G>A , CM000677.1:g.99452066G>A	GRCh37
NC_000015.8:g.97269589G>A	NCBI36
NG_009492.1:g.264306G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1400G>A	ENSP00000496919.1:p.Gly467Glu
ENST00000650285.1:c.1400G>A MANE Select	ENSP00000497069.1:p.Gly467Glu
ENST00000268035.10:c.1400G>A	ENSP00000268035.6:p.Gly467Glu
ENST00000558762.5:c.1400G>A	ENSP00000453007.1:p.Gly467Glu
ENST00000558898.1:c.491G>A	ENSP00000454115.1:p.Gly164Glu
ENST00000559582.1:n.307G>A
ENST00000559925.5:n.1400G>A
NM_000875.4:c.1400G>A	NP_000866.1:p.Gly467Glu
NM_001291858.1:c.1400G>A	NP_001278787.1:p.Gly467Glu
XM_011521513.1:c.1463G>A	XP_011519815.1:p.Gly488Glu
XM_011521514.1:c.1463G>A	XP_011519816.1:p.Gly488Glu
XM_011521515.1:c.1463G>A	XP_011519817.1:p.Gly488Glu
XM_011521516.1:c.491G>A	XP_011519818.1:p.Gly164Glu
XM_011521517.1:c.65G>A	XP_011519819.1:p.Gly22Glu
XM_011521516.2:c.491G>A	XP_011519818.1:p.Gly164Glu
XM_011521517.2:c.65G>A	XP_011519819.1:p.Gly22Glu
XM_017022136.1:c.1475G>A	XP_016877625.1:p.Gly492Glu
XM_017022137.1:c.1475G>A	XP_016877626.1:p.Gly492Glu
XM_017022138.1:c.1475G>A	XP_016877627.1:p.Gly492Glu
XM_017022139.1:c.1037G>A	XP_016877628.1:p.Gly346Glu
XM_024449913.1:c.491G>A	XP_024305681.1:p.Gly164Glu
NM_000875.5:c.1400G>A MANE Select	NP_000866.1:p.Gly467Glu
NM_001291858.2:c.1400G>A	NP_001278787.1:p.Gly467Glu