Canonical Allele Identifier: CA393696816
Gene: IGF1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98707696A>G , CM000677.2:g.98707696A>G GRCh38
NC_000015.9:g.99250925A>G , CM000677.1:g.99250925A>G GRCh37
NC_000015.8:g.97068448A>G NCBI36
NG_009492.1:g.63165A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.229A>G ENSP00000496919.1:p.Lys77Glu
ENST00000650285.1:c.229A>G MANE Select ENSP00000497069.1:p.Lys77Glu
ENST00000268035.10:c.229A>G ENSP00000268035.6:p.Lys77Glu
ENST00000558762.5:c.229A>G ENSP00000453007.1:p.Lys77Glu
ENST00000559925.5:n.229A>G
NM_000875.4:c.229A>G NP_000866.1:p.Lys77Glu
NM_001291858.1:c.229A>G NP_001278787.1:p.Lys77Glu
XM_011521513.1:c.229A>G XP_011519815.1:p.Lys77Glu
XM_011521514.1:c.229A>G XP_011519816.1:p.Lys77Glu
XM_011521515.1:c.229A>G XP_011519817.1:p.Lys77Glu
XM_017022136.1:c.304A>G XP_016877625.1:p.Lys102Glu
XM_017022137.1:c.304A>G XP_016877626.1:p.Lys102Glu
XM_017022138.1:c.304A>G XP_016877627.1:p.Lys102Glu
XM_017022139.1:c.-135A>G XP_016877628.1:n.-135A>G
NM_000875.5:c.229A>G MANE Select NP_000866.1:p.Lys77Glu
NM_001291858.2:c.229A>G NP_001278787.1:p.Lys77Glu