Canonical Allele Identifier: CA393697198

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99251097G>T (hg19) ; chr15:g.98707868G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707868G>T , CM000677.2:g.98707868G>T	GRCh38
NC_000015.9:g.99251097G>T , CM000677.1:g.99251097G>T	GRCh37
NC_000015.8:g.97068620G>T	NCBI36
NG_009492.1:g.63337G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.401G>T	ENSP00000496919.1:p.Arg134Met
ENST00000650285.1:c.401G>T MANE Select	ENSP00000497069.1:p.Arg134Met
ENST00000268035.10:c.401G>T	ENSP00000268035.6:p.Arg134Met
ENST00000558355.1:c.38G>T	ENSP00000453630.1:p.Arg13Met
ENST00000558762.5:c.401G>T	ENSP00000453007.1:p.Arg134Met
ENST00000559925.5:n.401G>T
NM_000875.4:c.401G>T	NP_000866.1:p.Arg134Met
NM_001291858.1:c.401G>T	NP_001278787.1:p.Arg134Met
XM_011521513.1:c.401G>T	XP_011519815.1:p.Arg134Met
XM_011521514.1:c.401G>T	XP_011519816.1:p.Arg134Met
XM_011521515.1:c.401G>T	XP_011519817.1:p.Arg134Met
XM_017022136.1:c.476G>T	XP_016877625.1:p.Arg159Met
XM_017022137.1:c.476G>T	XP_016877626.1:p.Arg159Met
XM_017022138.1:c.476G>T	XP_016877627.1:p.Arg159Met
XM_017022139.1:c.38G>T	XP_016877628.1:p.Arg13Met
NM_000875.5:c.401G>T MANE Select	NP_000866.1:p.Arg134Met
NM_001291858.2:c.401G>T	NP_001278787.1:p.Arg134Met