Canonical Allele Identifier: CA2805415478

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908947_98908948insCACCCAAACACACCCAAC , CM000677.2:g.98908947_98908948insCACCCAAACACACCCAAC	GRCh38
NC_000015.9:g.99452176_99452177insCACCCAAACACACCCAAC , CM000677.1:g.99452176_99452177insCACCCAAACACACCCAAC	GRCh37
NC_000015.8:g.97269699_97269700insCACCCAAACACACCCAAC	NCBI36
NG_009492.1:g.264416_264417insCACCCAAACACACCCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1462+48_1462+49insCACCCAAACACACCCAAC	ENSP00000496919.1:n.1462+48_1462+49insCACCCAAACACACCCAAC
ENST00000650285.1:c.1462+48_1462+49insCACCCAAACACACCCAAC MANE Select	ENSP00000497069.1:n.1462+48_1462+49insCACCCAAACACACCCAAC
ENST00000268035.10:c.1462+48_1462+49insCACCCAAACACACCCAAC	ENSP00000268035.6:n.1462+48_1462+49insCACCCAAACACACCCAAC
ENST00000558762.5:c.1462+48_1462+49insCACCCAAACACACCCAAC	ENSP00000453007.1:n.1462+48_1462+49insCACCCAAACACACCCAAC
ENST00000558898.1:c.553+48_553+49insCACCCAAACACACCCAAC	ENSP00000454115.1:n.553+48_553+49insCACCCAAACACACCCAAC
ENST00000559582.1:n.369+48_369+49insCACCCAAACACACCCAAC
ENST00000559925.5:n.1462+48_1462+49insCACCCAAACACACCCAAC
NM_000875.4:c.1462+48_1462+49insCACCCAAACACACCCAAC	NP_000866.1:n.1462+48_1462+49insCACCCAAACACACCCAAC
NM_001291858.1:c.1462+48_1462+49insCACCCAAACACACCCAAC	NP_001278787.1:n.1462+48_1462+49insCACCCAAACACACCCAAC
XM_011521513.1:c.1525+48_1525+49insCACCCAAACACACCCAAC	XP_011519815.1:n.1525+48_1525+49insCACCCAAACACACCCAAC
XM_011521514.1:c.1525+48_1525+49insCACCCAAACACACCCAAC	XP_011519816.1:n.1525+48_1525+49insCACCCAAACACACCCAAC
XM_011521515.1:c.1525+48_1525+49insCACCCAAACACACCCAAC	XP_011519817.1:n.1525+48_1525+49insCACCCAAACACACCCAAC
XM_011521516.1:c.553+48_553+49insCACCCAAACACACCCAAC	XP_011519818.1:n.553+48_553+49insCACCCAAACACACCCAAC
XM_011521517.1:c.127+48_127+49insCACCCAAACACACCCAAC	XP_011519819.1:n.127+48_127+49insCACCCAAACACACCCAAC
XM_011521516.2:c.553+48_553+49insCACCCAAACACACCCAAC	XP_011519818.1:n.553+48_553+49insCACCCAAACACACCCAAC
XM_011521517.2:c.127+48_127+49insCACCCAAACACACCCAAC	XP_011519819.1:n.127+48_127+49insCACCCAAACACACCCAAC
XM_017022136.1:c.1537+48_1537+49insCACCCAAACACACCCAAC	XP_016877625.1:n.1537+48_1537+49insCACCCAAACACACCCAAC
XM_017022137.1:c.1537+48_1537+49insCACCCAAACACACCCAAC	XP_016877626.1:n.1537+48_1537+49insCACCCAAACACACCCAAC
XM_017022138.1:c.1537+48_1537+49insCACCCAAACACACCCAAC	XP_016877627.1:n.1537+48_1537+49insCACCCAAACACACCCAAC
XM_017022139.1:c.1099+48_1099+49insCACCCAAACACACCCAAC	XP_016877628.1:n.1099+48_1099+49insCACCCAAACACACCCAAC
XM_024449913.1:c.553+48_553+49insCACCCAAACACACCCAAC	XP_024305681.1:n.553+48_553+49insCACCCAAACACACCCAAC
NM_000875.5:c.1462+48_1462+49insCACCCAAACACACCCAAC MANE Select	NP_000866.1:n.1462+48_1462+49insCACCCAAACACACCCAAC
NM_001291858.2:c.1462+48_1462+49insCACCCAAACACACCCAAC	NP_001278787.1:n.1462+48_1462+49insCACCCAAACACACCCAAC