Canonical Allele Identifier: CA2199282190

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908986_98908987delinsGC , CM000677.2:g.98908986_98908987delinsGC	GRCh38
NC_000015.9:g.99452215_99452216delinsGC , CM000677.1:g.99452215_99452216delinsGC	GRCh37
NC_000015.8:g.97269738_97269739delinsGC	NCBI36
NG_009492.1:g.264455_264456delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1462+87_1462+88delinsGC	ENSP00000496919.1:n.1462+87_1462+88delinsGC
ENST00000650285.1:c.1462+87_1462+88delinsGC MANE Select	ENSP00000497069.1:n.1462+87_1462+88delinsGC
ENST00000268035.10:c.1462+87_1462+88delinsGC	ENSP00000268035.6:n.1462+87_1462+88delinsGC
ENST00000558762.5:c.1462+87_1462+88delinsGC	ENSP00000453007.1:n.1462+87_1462+88delinsGC
ENST00000558898.1:c.553+87_553+88delinsGC	ENSP00000454115.1:n.553+87_553+88delinsGC
ENST00000559582.1:n.369+87_369+88delinsGC
ENST00000559925.5:n.1462+87_1462+88delinsGC
NM_000875.4:c.1462+87_1462+88delinsGC	NP_000866.1:n.1462+87_1462+88delinsGC
NM_001291858.1:c.1462+87_1462+88delinsGC	NP_001278787.1:n.1462+87_1462+88delinsGC
XM_011521513.1:c.1525+87_1525+88delinsGC	XP_011519815.1:n.1525+87_1525+88delinsGC
XM_011521514.1:c.1525+87_1525+88delinsGC	XP_011519816.1:n.1525+87_1525+88delinsGC
XM_011521515.1:c.1525+87_1525+88delinsGC	XP_011519817.1:n.1525+87_1525+88delinsGC
XM_011521516.1:c.553+87_553+88delinsGC	XP_011519818.1:n.553+87_553+88delinsGC
XM_011521517.1:c.127+87_127+88delinsGC	XP_011519819.1:n.127+87_127+88delinsGC
XM_011521516.2:c.553+87_553+88delinsGC	XP_011519818.1:n.553+87_553+88delinsGC
XM_011521517.2:c.127+87_127+88delinsGC	XP_011519819.1:n.127+87_127+88delinsGC
XM_017022136.1:c.1537+87_1537+88delinsGC	XP_016877625.1:n.1537+87_1537+88delinsGC
XM_017022137.1:c.1537+87_1537+88delinsGC	XP_016877626.1:n.1537+87_1537+88delinsGC
XM_017022138.1:c.1537+87_1537+88delinsGC	XP_016877627.1:n.1537+87_1537+88delinsGC
XM_017022139.1:c.1099+87_1099+88delinsGC	XP_016877628.1:n.1099+87_1099+88delinsGC
XM_024449913.1:c.553+87_553+88delinsGC	XP_024305681.1:n.553+87_553+88delinsGC
NM_000875.5:c.1462+87_1462+88delinsGC MANE Select	NP_000866.1:n.1462+87_1462+88delinsGC
NM_001291858.2:c.1462+87_1462+88delinsGC	NP_001278787.1:n.1462+87_1462+88delinsGC