Canonical Allele Identifier: CA2199300883
Gene: IGF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98962599A= , CM000677.2:g.98962599A= GRCh38
NC_000015.9:g.99505828A= , CM000677.1:g.99505828A= GRCh37
NC_000015.8:g.97323351A= NCBI36
NG_009492.1:g.318068A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.*5157A= ENSP00000496919.1:n.*5157A=
ENST00000650285.1:c.*5157A= MANE Select ENSP00000497069.1:n.*5157A=
ENST00000268035.10:c.*5157A= ENSP00000268035.6:n.*5157A=
ENST00000558762.5:c.*5157A= ENSP00000453007.1:n.*5157A=
NM_000875.4:c.*5157A= NP_000866.1:n.*5157A=
NM_001291858.1:c.*5157A= NP_001278787.1:n.*5157A=
XM_011521513.1:c.*5157A= XP_011519815.1:n.*5157A=
XM_011521514.1:c.*4671A= XP_011519816.1:n.*4671A=
XM_011521515.1:c.*5157A= XP_011519817.1:n.*5157A=
XM_011521516.1:c.*5157A= XP_011519818.1:n.*5157A=
XM_011521517.1:c.*5157A= XP_011519819.1:n.*5157A=
XM_017022136.1:c.*5157A= XP_016877625.1:n.*5157A=
XM_017022137.1:c.*4671A= XP_016877626.1:n.*4671A=
XM_017022138.1:c.*5157A= XP_016877627.1:n.*5157A=
NM_000875.5:c.*5157A= MANE Select NP_000866.1:n.*5157A=
NM_001291858.2:c.*5157A= NP_001278787.1:n.*5157A=