Canonical Allele Identifier: CA2199282083
Gene: IGF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98908889G= , CM000677.2:g.98908889G= GRCh38
NC_000015.9:g.99452118G= , CM000677.1:g.99452118G= GRCh37
NC_000015.8:g.97269641G= NCBI36
NG_009492.1:g.264358G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.1452G= ENSP00000496919.1:p.Glu484=
ENST00000650285.1:c.1452G= MANE Select ENSP00000497069.1:p.Glu484=
ENST00000268035.10:c.1452G= ENSP00000268035.6:p.Glu484=
ENST00000558762.5:c.1452G= ENSP00000453007.1:p.Glu484=
ENST00000558898.1:c.543G= ENSP00000454115.1:p.Glu181=
ENST00000559582.1:n.359G=
ENST00000559925.5:n.1452G=
NM_000875.4:c.1452G= NP_000866.1:p.Glu484=
NM_001291858.1:c.1452G= NP_001278787.1:p.Glu484=
XM_011521513.1:c.1515G= XP_011519815.1:p.Glu505=
XM_011521514.1:c.1515G= XP_011519816.1:p.Glu505=
XM_011521515.1:c.1515G= XP_011519817.1:p.Glu505=
XM_011521516.1:c.543G= XP_011519818.1:p.Glu181=
XM_011521517.1:c.117G= XP_011519819.1:p.Glu39=
XM_011521516.2:c.543G= XP_011519818.1:p.Glu181=
XM_011521517.2:c.117G= XP_011519819.1:p.Glu39=
XM_017022136.1:c.1527G= XP_016877625.1:p.Glu509=
XM_017022137.1:c.1527G= XP_016877626.1:p.Glu509=
XM_017022138.1:c.1527G= XP_016877627.1:p.Glu509=
XM_017022139.1:c.1089G= XP_016877628.1:p.Glu363=
XM_024449913.1:c.543G= XP_024305681.1:p.Glu181=
NM_000875.5:c.1452G= MANE Select NP_000866.1:p.Glu484=
NM_001291858.2:c.1452G= NP_001278787.1:p.Glu484=