Canonical Allele Identifier: CA393675546
Gene: IGF1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98908785T>A , CM000677.2:g.98908785T>A GRCh38
NC_000015.9:g.99452014T>A , CM000677.1:g.99452014T>A GRCh37
NC_000015.8:g.97269537T>A NCBI36
NG_009492.1:g.264254T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.1348T>A ENSP00000496919.1:p.Phe450Ile
ENST00000650285.1:c.1348T>A MANE Select ENSP00000497069.1:p.Phe450Ile
ENST00000268035.10:c.1348T>A ENSP00000268035.6:p.Phe450Ile
ENST00000558762.5:c.1348T>A ENSP00000453007.1:p.Phe450Ile
ENST00000558898.1:c.439T>A ENSP00000454115.1:p.Phe147Ile
ENST00000559582.1:n.255T>A
ENST00000559925.5:n.1348T>A
NM_000875.4:c.1348T>A NP_000866.1:p.Phe450Ile
NM_001291858.1:c.1348T>A NP_001278787.1:p.Phe450Ile
XM_011521513.1:c.1411T>A XP_011519815.1:p.Phe471Ile
XM_011521514.1:c.1411T>A XP_011519816.1:p.Phe471Ile
XM_011521515.1:c.1411T>A XP_011519817.1:p.Phe471Ile
XM_011521516.1:c.439T>A XP_011519818.1:p.Phe147Ile
XM_011521517.1:c.13T>A XP_011519819.1:p.Phe5Ile
XM_011521516.2:c.439T>A XP_011519818.1:p.Phe147Ile
XM_011521517.2:c.13T>A XP_011519819.1:p.Phe5Ile
XM_017022136.1:c.1423T>A XP_016877625.1:p.Phe475Ile
XM_017022137.1:c.1423T>A XP_016877626.1:p.Phe475Ile
XM_017022138.1:c.1423T>A XP_016877627.1:p.Phe475Ile
XM_017022139.1:c.985T>A XP_016877628.1:p.Phe329Ile
XM_024449913.1:c.439T>A XP_024305681.1:p.Phe147Ile
NM_000875.5:c.1348T>A MANE Select NP_000866.1:p.Phe450Ile
NM_001291858.2:c.1348T>A NP_001278787.1:p.Phe450Ile