Canonical Allele Identifier: CA2199282124

Gene: IGF1R

Linked Data

• dbSNP Id: rs2014859836

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908927_98908934del , CM000677.2:g.98908927_98908934del	GRCh38
NC_000015.9:g.99452156_99452163del , CM000677.1:g.99452156_99452163del	GRCh37
NC_000015.8:g.97269679_97269686del	NCBI36
NG_009492.1:g.264396_264403del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1462+28_1462+35del	ENSP00000496919.1:n.1462+28_1462+35del
ENST00000650285.1:c.1462+28_1462+35del MANE Select	ENSP00000497069.1:n.1462+28_1462+35del
ENST00000268035.10:c.1462+28_1462+35del	ENSP00000268035.6:n.1462+28_1462+35del
ENST00000558762.5:c.1462+28_1462+35del	ENSP00000453007.1:n.1462+28_1462+35del
ENST00000558898.1:c.553+28_553+35del	ENSP00000454115.1:n.553+28_553+35del
ENST00000559582.1:n.369+28_369+35del
ENST00000559925.5:n.1462+28_1462+35del
NM_000875.4:c.1462+28_1462+35del	NP_000866.1:n.1462+28_1462+35del
NM_001291858.1:c.1462+28_1462+35del	NP_001278787.1:n.1462+28_1462+35del
XM_011521513.1:c.1525+28_1525+35del	XP_011519815.1:n.1525+28_1525+35del
XM_011521514.1:c.1525+28_1525+35del	XP_011519816.1:n.1525+28_1525+35del
XM_011521515.1:c.1525+28_1525+35del	XP_011519817.1:n.1525+28_1525+35del
XM_011521516.1:c.553+28_553+35del	XP_011519818.1:n.553+28_553+35del
XM_011521517.1:c.127+28_127+35del	XP_011519819.1:n.127+28_127+35del
XM_011521516.2:c.553+28_553+35del	XP_011519818.1:n.553+28_553+35del
XM_011521517.2:c.127+28_127+35del	XP_011519819.1:n.127+28_127+35del
XM_017022136.1:c.1537+28_1537+35del	XP_016877625.1:n.1537+28_1537+35del
XM_017022137.1:c.1537+28_1537+35del	XP_016877626.1:n.1537+28_1537+35del
XM_017022138.1:c.1537+28_1537+35del	XP_016877627.1:n.1537+28_1537+35del
XM_017022139.1:c.1099+28_1099+35del	XP_016877628.1:n.1099+28_1099+35del
XM_024449913.1:c.553+28_553+35del	XP_024305681.1:n.553+28_553+35del
NM_000875.5:c.1462+28_1462+35del MANE Select	NP_000866.1:n.1462+28_1462+35del
NM_001291858.2:c.1462+28_1462+35del	NP_001278787.1:n.1462+28_1462+35del