Canonical Allele Identifier: CA393697041
Gene: IGF1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98707799T>C , CM000677.2:g.98707799T>C GRCh38
NC_000015.9:g.99251028T>C , CM000677.1:g.99251028T>C GRCh37
NC_000015.8:g.97068551T>C NCBI36
NG_009492.1:g.63268T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649865.1:c.332T>C ENSP00000496919.1:p.Leu111Pro
ENST00000650285.1:c.332T>C MANE Select ENSP00000497069.1:p.Leu111Pro
ENST00000268035.10:c.332T>C ENSP00000268035.6:p.Leu111Pro
ENST00000558762.5:c.332T>C ENSP00000453007.1:p.Leu111Pro
ENST00000559925.5:n.332T>C
NM_000875.4:c.332T>C NP_000866.1:p.Leu111Pro
NM_001291858.1:c.332T>C NP_001278787.1:p.Leu111Pro
XM_011521513.1:c.332T>C XP_011519815.1:p.Leu111Pro
XM_011521514.1:c.332T>C XP_011519816.1:p.Leu111Pro
XM_011521515.1:c.332T>C XP_011519817.1:p.Leu111Pro
XM_017022136.1:c.407T>C XP_016877625.1:p.Leu136Pro
XM_017022137.1:c.407T>C XP_016877626.1:p.Leu136Pro
XM_017022138.1:c.407T>C XP_016877627.1:p.Leu136Pro
XM_017022139.1:c.-32T>C XP_016877628.1:n.-32T>C
NM_000875.5:c.332T>C MANE Select NP_000866.1:p.Leu111Pro
NM_001291858.2:c.332T>C NP_001278787.1:p.Leu111Pro