Canonical Allele Identifier: CA2199282147

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908938_98908941delinsCATG , CM000677.2:g.98908938_98908941delinsCATG	GRCh38
NC_000015.9:g.99452167_99452170delinsCATG , CM000677.1:g.99452167_99452170delinsCATG	GRCh37
NC_000015.8:g.97269690_97269693delinsCATG	NCBI36
NG_009492.1:g.264407_264410delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1462+39_1462+42delinsCATG	ENSP00000496919.1:n.1462+39_1462+42delinsCATG
ENST00000650285.1:c.1462+39_1462+42delinsCATG MANE Select	ENSP00000497069.1:n.1462+39_1462+42delinsCATG
ENST00000268035.10:c.1462+39_1462+42delinsCATG	ENSP00000268035.6:n.1462+39_1462+42delinsCATG
ENST00000558762.5:c.1462+39_1462+42delinsCATG	ENSP00000453007.1:n.1462+39_1462+42delinsCATG
ENST00000558898.1:c.553+39_553+42delinsCATG	ENSP00000454115.1:n.553+39_553+42delinsCATG
ENST00000559582.1:n.369+39_369+42delinsCATG
ENST00000559925.5:n.1462+39_1462+42delinsCATG
NM_000875.4:c.1462+39_1462+42delinsCATG	NP_000866.1:n.1462+39_1462+42delinsCATG
NM_001291858.1:c.1462+39_1462+42delinsCATG	NP_001278787.1:n.1462+39_1462+42delinsCATG
XM_011521513.1:c.1525+39_1525+42delinsCATG	XP_011519815.1:n.1525+39_1525+42delinsCATG
XM_011521514.1:c.1525+39_1525+42delinsCATG	XP_011519816.1:n.1525+39_1525+42delinsCATG
XM_011521515.1:c.1525+39_1525+42delinsCATG	XP_011519817.1:n.1525+39_1525+42delinsCATG
XM_011521516.1:c.553+39_553+42delinsCATG	XP_011519818.1:n.553+39_553+42delinsCATG
XM_011521517.1:c.127+39_127+42delinsCATG	XP_011519819.1:n.127+39_127+42delinsCATG
XM_011521516.2:c.553+39_553+42delinsCATG	XP_011519818.1:n.553+39_553+42delinsCATG
XM_011521517.2:c.127+39_127+42delinsCATG	XP_011519819.1:n.127+39_127+42delinsCATG
XM_017022136.1:c.1537+39_1537+42delinsCATG	XP_016877625.1:n.1537+39_1537+42delinsCATG
XM_017022137.1:c.1537+39_1537+42delinsCATG	XP_016877626.1:n.1537+39_1537+42delinsCATG
XM_017022138.1:c.1537+39_1537+42delinsCATG	XP_016877627.1:n.1537+39_1537+42delinsCATG
XM_017022139.1:c.1099+39_1099+42delinsCATG	XP_016877628.1:n.1099+39_1099+42delinsCATG
XM_024449913.1:c.553+39_553+42delinsCATG	XP_024305681.1:n.553+39_553+42delinsCATG
NM_000875.5:c.1462+39_1462+42delinsCATG MANE Select	NP_000866.1:n.1462+39_1462+42delinsCATG
NM_001291858.2:c.1462+39_1462+42delinsCATG	NP_001278787.1:n.1462+39_1462+42delinsCATG