Canonical Allele Identifier: CA7752082
Gene: IGF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 1956433
ClinVar RCV Id: RCV002700841
dbSNP Id: rs763660010

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98908849G>A , CM000677.2:g.98908849G>A GRCh38
NC_000015.9:g.99452078G>A , CM000677.1:g.99452078G>A GRCh37
NC_000015.8:g.97269601G>A NCBI36
NG_009492.1:g.264318G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.1412G>A ENSP00000496919.1:p.Arg471His
ENST00000650285.1:c.1412G>A MANE Select ENSP00000497069.1:p.Arg471His
ENST00000268035.10:c.1412G>A ENSP00000268035.6:p.Arg471His
ENST00000558762.5:c.1412G>A ENSP00000453007.1:p.Arg471His
ENST00000558898.1:c.503G>A ENSP00000454115.1:p.Arg168His
ENST00000559582.1:n.319G>A
ENST00000559925.5:n.1412G>A
NM_000875.4:c.1412G>A NP_000866.1:p.Arg471His
NM_001291858.1:c.1412G>A NP_001278787.1:p.Arg471His
XM_011521513.1:c.1475G>A XP_011519815.1:p.Arg492His
XM_011521514.1:c.1475G>A XP_011519816.1:p.Arg492His
XM_011521515.1:c.1475G>A XP_011519817.1:p.Arg492His
XM_011521516.1:c.503G>A XP_011519818.1:p.Arg168His
XM_011521517.1:c.77G>A XP_011519819.1:p.Arg26His
XM_011521516.2:c.503G>A XP_011519818.1:p.Arg168His
XM_011521517.2:c.77G>A XP_011519819.1:p.Arg26His
XM_017022136.1:c.1487G>A XP_016877625.1:p.Arg496His
XM_017022137.1:c.1487G>A XP_016877626.1:p.Arg496His
XM_017022138.1:c.1487G>A XP_016877627.1:p.Arg496His
XM_017022139.1:c.1049G>A XP_016877628.1:p.Arg350His
XM_024449913.1:c.503G>A XP_024305681.1:p.Arg168His
NM_000875.5:c.1412G>A MANE Select NP_000866.1:p.Arg471His
NM_001291858.2:c.1412G>A NP_001278787.1:p.Arg471His