Canonical Allele Identifier: CA2199287469
Gene: IGF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98912965A= , CM000677.2:g.98912965A= GRCh38
NC_000015.9:g.99456194A= , CM000677.1:g.99456194A= GRCh37
NC_000015.8:g.97273717A= NCBI36
NG_009492.1:g.268434A=

Transcript Alleles

HGVS Amino-acid change
ENST00000649865.1:c.1590-79A= ENSP00000496919.1:n.1590-79A=
ENST00000650285.1:c.1590-79A= MANE Select ENSP00000497069.1:n.1590-79A=
ENST00000268035.10:c.1590-79A= ENSP00000268035.6:n.1590-79A=
ENST00000558762.5:c.1590-79A= ENSP00000453007.1:n.1590-79A=
ENST00000559582.1:n.497-79A=
ENST00000559925.5:n.1590-79A=
NM_000875.4:c.1590-79A= NP_000866.1:n.1590-79A=
NM_001291858.1:c.1590-79A= NP_001278787.1:n.1590-79A=
XM_011521513.1:c.1653-79A= XP_011519815.1:n.1653-79A=
XM_011521514.1:c.1653-79A= XP_011519816.1:n.1653-79A=
XM_011521515.1:c.1653-79A= XP_011519817.1:n.1653-79A=
XM_011521516.1:c.681-79A= XP_011519818.1:n.681-79A=
XM_011521517.1:c.255-79A= XP_011519819.1:n.255-79A=
XM_011521516.2:c.681-79A= XP_011519818.1:n.681-79A=
XM_011521517.2:c.255-79A= XP_011519819.1:n.255-79A=
XM_017022136.1:c.1665-79A= XP_016877625.1:n.1665-79A=
XM_017022137.1:c.1665-79A= XP_016877626.1:n.1665-79A=
XM_017022138.1:c.1665-79A= XP_016877627.1:n.1665-79A=
XM_017022139.1:c.1227-79A= XP_016877628.1:n.1227-79A=
XM_024449913.1:c.681-79A= XP_024305681.1:n.681-79A=
NM_000875.5:c.1590-79A= MANE Select NP_000866.1:n.1590-79A=
NM_001291858.2:c.1590-79A= NP_001278787.1:n.1590-79A=