Canonical Allele Identifier: CA393676183
Gene: IGF1R HGNC NCBI

Linked Data

dbSNP Id: rs1441621301

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98908848C>G , CM000677.2:g.98908848C>G GRCh38
NC_000015.9:g.99452077C>G , CM000677.1:g.99452077C>G GRCh37
NC_000015.8:g.97269600C>G NCBI36
NG_009492.1:g.264317C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.1411C>G ENSP00000496919.1:p.Arg471Gly
ENST00000650285.1:c.1411C>G MANE Select ENSP00000497069.1:p.Arg471Gly
ENST00000268035.10:c.1411C>G ENSP00000268035.6:p.Arg471Gly
ENST00000558762.5:c.1411C>G ENSP00000453007.1:p.Arg471Gly
ENST00000558898.1:c.502C>G ENSP00000454115.1:p.Arg168Gly
ENST00000559582.1:n.318C>G
ENST00000559925.5:n.1411C>G
NM_000875.4:c.1411C>G NP_000866.1:p.Arg471Gly
NM_001291858.1:c.1411C>G NP_001278787.1:p.Arg471Gly
XM_011521513.1:c.1474C>G XP_011519815.1:p.Arg492Gly
XM_011521514.1:c.1474C>G XP_011519816.1:p.Arg492Gly
XM_011521515.1:c.1474C>G XP_011519817.1:p.Arg492Gly
XM_011521516.1:c.502C>G XP_011519818.1:p.Arg168Gly
XM_011521517.1:c.76C>G XP_011519819.1:p.Arg26Gly
XM_011521516.2:c.502C>G XP_011519818.1:p.Arg168Gly
XM_011521517.2:c.76C>G XP_011519819.1:p.Arg26Gly
XM_017022136.1:c.1486C>G XP_016877625.1:p.Arg496Gly
XM_017022137.1:c.1486C>G XP_016877626.1:p.Arg496Gly
XM_017022138.1:c.1486C>G XP_016877627.1:p.Arg496Gly
XM_017022139.1:c.1048C>G XP_016877628.1:p.Arg350Gly
XM_024449913.1:c.502C>G XP_024305681.1:p.Arg168Gly
NM_000875.5:c.1411C>G MANE Select NP_000866.1:p.Arg471Gly
NM_001291858.2:c.1411C>G NP_001278787.1:p.Arg471Gly