Canonical Allele Identifier: CA393676088
Gene: IGF1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98908836G>C , CM000677.2:g.98908836G>C GRCh38
NC_000015.9:g.99452065G>C , CM000677.1:g.99452065G>C GRCh37
NC_000015.8:g.97269588G>C NCBI36
NG_009492.1:g.264305G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.1399G>C ENSP00000496919.1:p.Gly467Arg
ENST00000650285.1:c.1399G>C MANE Select ENSP00000497069.1:p.Gly467Arg
ENST00000268035.10:c.1399G>C ENSP00000268035.6:p.Gly467Arg
ENST00000558762.5:c.1399G>C ENSP00000453007.1:p.Gly467Arg
ENST00000558898.1:c.490G>C ENSP00000454115.1:p.Gly164Arg
ENST00000559582.1:n.306G>C
ENST00000559925.5:n.1399G>C
NM_000875.4:c.1399G>C NP_000866.1:p.Gly467Arg
NM_001291858.1:c.1399G>C NP_001278787.1:p.Gly467Arg
XM_011521513.1:c.1462G>C XP_011519815.1:p.Gly488Arg
XM_011521514.1:c.1462G>C XP_011519816.1:p.Gly488Arg
XM_011521515.1:c.1462G>C XP_011519817.1:p.Gly488Arg
XM_011521516.1:c.490G>C XP_011519818.1:p.Gly164Arg
XM_011521517.1:c.64G>C XP_011519819.1:p.Gly22Arg
XM_011521516.2:c.490G>C XP_011519818.1:p.Gly164Arg
XM_011521517.2:c.64G>C XP_011519819.1:p.Gly22Arg
XM_017022136.1:c.1474G>C XP_016877625.1:p.Gly492Arg
XM_017022137.1:c.1474G>C XP_016877626.1:p.Gly492Arg
XM_017022138.1:c.1474G>C XP_016877627.1:p.Gly492Arg
XM_017022139.1:c.1036G>C XP_016877628.1:p.Gly346Arg
XM_024449913.1:c.490G>C XP_024305681.1:p.Gly164Arg
NM_000875.5:c.1399G>C MANE Select NP_000866.1:p.Gly467Arg
NM_001291858.2:c.1399G>C NP_001278787.1:p.Gly467Arg