Canonical Allele Identifier: CA2199177316
Gene: IGF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98707714G= , CM000677.2:g.98707714G= GRCh38
NC_000015.9:g.99250943G= , CM000677.1:g.99250943G= GRCh37
NC_000015.8:g.97068466G= NCBI36
NG_009492.1:g.63183G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.247G= ENSP00000496919.1:p.Glu83=
ENST00000650285.1:c.247G= MANE Select ENSP00000497069.1:p.Glu83=
ENST00000268035.10:c.247G= ENSP00000268035.6:p.Glu83=
ENST00000558762.5:c.247G= ENSP00000453007.1:p.Glu83=
ENST00000559925.5:n.247G=
NM_000875.4:c.247G= NP_000866.1:p.Glu83=
NM_001291858.1:c.247G= NP_001278787.1:p.Glu83=
XM_011521513.1:c.247G= XP_011519815.1:p.Glu83=
XM_011521514.1:c.247G= XP_011519816.1:p.Glu83=
XM_011521515.1:c.247G= XP_011519817.1:p.Glu83=
XM_017022136.1:c.322G= XP_016877625.1:p.Glu108=
XM_017022137.1:c.322G= XP_016877626.1:p.Glu108=
XM_017022138.1:c.322G= XP_016877627.1:p.Glu108=
XM_017022139.1:c.-117G= XP_016877628.1:n.-117G=
NM_000875.5:c.247G= MANE Select NP_000866.1:p.Glu83=
NM_001291858.2:c.247G= NP_001278787.1:p.Glu83=