Canonical Allele Identifier: CA393679009

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99456374C>G (hg19) ; chr15:g.98913145C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98913145C>G , CM000677.2:g.98913145C>G	GRCh38
NC_000015.9:g.99456374C>G , CM000677.1:g.99456374C>G	GRCh37
NC_000015.8:g.97273897C>G	NCBI36
NG_009492.1:g.268614C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1691C>G	ENSP00000496919.1:p.Pro564Arg
ENST00000650285.1:c.1691C>G MANE Select	ENSP00000497069.1:p.Pro564Arg
ENST00000268035.10:c.1691C>G	ENSP00000268035.6:p.Pro564Arg
ENST00000558762.5:c.1691C>G	ENSP00000453007.1:p.Pro564Arg
ENST00000559925.5:n.1691C>G
NM_000875.4:c.1691C>G	NP_000866.1:p.Pro564Arg
NM_001291858.1:c.1691C>G	NP_001278787.1:p.Pro564Arg
XM_011521513.1:c.1754C>G	XP_011519815.1:p.Pro585Arg
XM_011521514.1:c.1754C>G	XP_011519816.1:p.Pro585Arg
XM_011521515.1:c.1754C>G	XP_011519817.1:p.Pro585Arg
XM_011521516.1:c.782C>G	XP_011519818.1:p.Pro261Arg
XM_011521517.1:c.356C>G	XP_011519819.1:p.Pro119Arg
XM_011521516.2:c.782C>G	XP_011519818.1:p.Pro261Arg
XM_011521517.2:c.356C>G	XP_011519819.1:p.Pro119Arg
XM_017022136.1:c.1766C>G	XP_016877625.1:p.Pro589Arg
XM_017022137.1:c.1766C>G	XP_016877626.1:p.Pro589Arg
XM_017022138.1:c.1766C>G	XP_016877627.1:p.Pro589Arg
XM_017022139.1:c.1328C>G	XP_016877628.1:p.Pro443Arg
XM_024449913.1:c.782C>G	XP_024305681.1:p.Pro261Arg
NM_000875.5:c.1691C>G MANE Select	NP_000866.1:p.Pro564Arg
NM_001291858.2:c.1691C>G	NP_001278787.1:p.Pro564Arg