Canonical Allele Identifier: CA393674705

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99451931T>A (hg19) ; chr15:g.98908702T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908702T>A , CM000677.2:g.98908702T>A	GRCh38
NC_000015.9:g.99451931T>A , CM000677.1:g.99451931T>A	GRCh37
NC_000015.8:g.97269454T>A	NCBI36
NG_009492.1:g.264171T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1265T>A	ENSP00000496919.1:p.Val422Asp
ENST00000650285.1:c.1265T>A MANE Select	ENSP00000497069.1:p.Val422Asp
ENST00000268035.10:c.1265T>A	ENSP00000268035.6:p.Val422Asp
ENST00000558762.5:c.1265T>A	ENSP00000453007.1:p.Val422Asp
ENST00000558898.1:c.356T>A	ENSP00000454115.1:p.Val119Asp
ENST00000559582.1:n.172T>A
ENST00000559925.5:n.1265T>A
NM_000875.4:c.1265T>A	NP_000866.1:p.Val422Asp
NM_001291858.1:c.1265T>A	NP_001278787.1:p.Val422Asp
XM_011521513.1:c.1328T>A	XP_011519815.1:p.Val443Asp
XM_011521514.1:c.1328T>A	XP_011519816.1:p.Val443Asp
XM_011521515.1:c.1328T>A	XP_011519817.1:p.Val443Asp
XM_011521516.1:c.356T>A	XP_011519818.1:p.Val119Asp
XM_011521517.1:c.-71T>A	XP_011519819.1:n.-71T>A
XM_011521516.2:c.356T>A	XP_011519818.1:p.Val119Asp
XM_011521517.2:c.-71T>A	XP_011519819.1:n.-71T>A
XM_017022136.1:c.1340T>A	XP_016877625.1:p.Val447Asp
XM_017022137.1:c.1340T>A	XP_016877626.1:p.Val447Asp
XM_017022138.1:c.1340T>A	XP_016877627.1:p.Val447Asp
XM_017022139.1:c.902T>A	XP_016877628.1:p.Val301Asp
XM_024449913.1:c.356T>A	XP_024305681.1:p.Val119Asp
NM_000875.5:c.1265T>A MANE Select	NP_000866.1:p.Val422Asp
NM_001291858.2:c.1265T>A	NP_001278787.1:p.Val422Asp