Canonical Allele Identifier: CA393659002
Gene: IGF1R HGNC NCBI

Linked Data

dbSNP Id: rs2016102636

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98935383G>C , CM000677.2:g.98935383G>C GRCh38
NC_000015.9:g.99478612G>C , CM000677.1:g.99478612G>C GRCh37
NC_000015.8:g.97296135G>C NCBI36
NG_009492.1:g.290852G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.3251G>C ENSP00000496919.1:p.Gly1084Ala
ENST00000650285.1:c.3254G>C MANE Select ENSP00000497069.1:p.Gly1085Ala
ENST00000268035.10:c.3254G>C ENSP00000268035.6:p.Gly1085Ala
ENST00000558762.5:c.3251G>C ENSP00000453007.1:p.Gly1084Ala
NM_000875.4:c.3254G>C NP_000866.1:p.Gly1085Ala
NM_001291858.1:c.3251G>C NP_001278787.1:p.Gly1084Ala
XM_011521513.1:c.3317G>C XP_011519815.1:p.Gly1106Ala
XM_011521514.1:c.3317G>C XP_011519816.1:p.Gly1106Ala
XM_011521515.1:c.3314G>C XP_011519817.1:p.Gly1105Ala
XM_011521516.1:c.2345G>C XP_011519818.1:p.Gly782Ala
XM_011521517.1:c.1919G>C XP_011519819.1:p.Gly640Ala
XM_011521516.2:c.2345G>C XP_011519818.1:p.Gly782Ala
XM_011521517.2:c.1919G>C XP_011519819.1:p.Gly640Ala
XM_017022136.1:c.3329G>C XP_016877625.1:p.Gly1110Ala
XM_017022137.1:c.3329G>C XP_016877626.1:p.Gly1110Ala
XM_017022138.1:c.3326G>C XP_016877627.1:p.Gly1109Ala
XM_017022139.1:c.2891G>C XP_016877628.1:p.Gly964Ala
XM_024449913.1:c.2345G>C XP_024305681.1:p.Gly782Ala
NM_000875.5:c.3254G>C MANE Select NP_000866.1:p.Gly1085Ala
NM_001291858.2:c.3251G>C NP_001278787.1:p.Gly1084Ala