Canonical Allele Identifier: CA2199299345
Gene: IGF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98960571G>C , CM000677.2:g.98960571G>C GRCh38
NC_000015.9:g.99503800G>C , CM000677.1:g.99503800G>C GRCh37
NC_000015.8:g.97321323G>C NCBI36
NG_009492.1:g.316040G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.*3129G>C ENSP00000496919.1:n.*3129G>C
ENST00000650285.1:c.*3129G>C MANE Select ENSP00000497069.1:n.*3129G>C
ENST00000268035.10:c.*3129G>C ENSP00000268035.6:n.*3129G>C
ENST00000558762.5:c.*3129G>C ENSP00000453007.1:n.*3129G>C
NM_000875.4:c.*3129G>C NP_000866.1:n.*3129G>C
NM_001291858.1:c.*3129G>C NP_001278787.1:n.*3129G>C
XM_011521513.1:c.*3129G>C XP_011519815.1:n.*3129G>C
XM_011521514.1:c.*2643G>C XP_011519816.1:n.*2643G>C
XM_011521515.1:c.*3129G>C XP_011519817.1:n.*3129G>C
XM_011521516.1:c.*3129G>C XP_011519818.1:n.*3129G>C
XM_011521517.1:c.*3129G>C XP_011519819.1:n.*3129G>C
XM_017022136.1:c.*3129G>C XP_016877625.1:n.*3129G>C
XM_017022137.1:c.*2643G>C XP_016877626.1:n.*2643G>C
XM_017022138.1:c.*3129G>C XP_016877627.1:n.*3129G>C
NM_000875.5:c.*3129G>C MANE Select NP_000866.1:n.*3129G>C
NM_001291858.2:c.*3129G>C NP_001278787.1:n.*3129G>C