Canonical Allele Identifier: CA492324895

Gene: IGF1R

Linked Data

• dbSNP Id: rs752236741
• MyVariant Identifiers: chr15:g.99452064G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908835G>T , CM000677.2:g.98908835G>T	GRCh38
NC_000015.9:g.99452064G>T , CM000677.1:g.99452064G>T	GRCh37
NC_000015.8:g.97269587G>T	NCBI36
NG_009492.1:g.264304G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1398G>T	ENSP00000496919.1:p.Thr466=
ENST00000650285.1:c.1398G>T MANE Select	ENSP00000497069.1:p.Thr466=
ENST00000268035.10:c.1398G>T	ENSP00000268035.6:p.Thr466=
ENST00000558762.5:c.1398G>T	ENSP00000453007.1:p.Thr466=
ENST00000558898.1:c.489G>T	ENSP00000454115.1:p.Thr163=
ENST00000559582.1:n.305G>T
ENST00000559925.5:n.1398G>T
NM_000875.4:c.1398G>T	NP_000866.1:p.Thr466=
NM_001291858.1:c.1398G>T	NP_001278787.1:p.Thr466=
XM_011521513.1:c.1461G>T	XP_011519815.1:p.Thr487=
XM_011521514.1:c.1461G>T	XP_011519816.1:p.Thr487=
XM_011521515.1:c.1461G>T	XP_011519817.1:p.Thr487=
XM_011521516.1:c.489G>T	XP_011519818.1:p.Thr163=
XM_011521517.1:c.63G>T	XP_011519819.1:p.Thr21=
XM_011521516.2:c.489G>T	XP_011519818.1:p.Thr163=
XM_011521517.2:c.63G>T	XP_011519819.1:p.Thr21=
XM_017022136.1:c.1473G>T	XP_016877625.1:p.Thr491=
XM_017022137.1:c.1473G>T	XP_016877626.1:p.Thr491=
XM_017022138.1:c.1473G>T	XP_016877627.1:p.Thr491=
XM_017022139.1:c.1035G>T	XP_016877628.1:p.Thr345=
XM_024449913.1:c.489G>T	XP_024305681.1:p.Thr163=
NM_000875.5:c.1398G>T MANE Select	NP_000866.1:p.Thr466=
NM_001291858.2:c.1398G>T	NP_001278787.1:p.Thr466=