Canonical Allele Identifier: CA393696750

Gene: IGF1R

Linked Data

• dbSNP Id: rs2141258927
• MyVariant Identifiers: chr15:g.99250896C>A (hg19) ; chr15:g.98707667C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707667C>A , CM000677.2:g.98707667C>A	GRCh38
NC_000015.9:g.99250896C>A , CM000677.1:g.99250896C>A	GRCh37
NC_000015.8:g.97068419C>A	NCBI36
NG_009492.1:g.63136C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.200C>A	ENSP00000496919.1:p.Ala67Asp
ENST00000650285.1:c.200C>A MANE Select	ENSP00000497069.1:p.Ala67Asp
ENST00000268035.10:c.200C>A	ENSP00000268035.6:p.Ala67Asp
ENST00000558762.5:c.200C>A	ENSP00000453007.1:p.Ala67Asp
ENST00000559925.5:n.200C>A
NM_000875.4:c.200C>A	NP_000866.1:p.Ala67Asp
NM_001291858.1:c.200C>A	NP_001278787.1:p.Ala67Asp
XM_011521513.1:c.200C>A	XP_011519815.1:p.Ala67Asp
XM_011521514.1:c.200C>A	XP_011519816.1:p.Ala67Asp
XM_011521515.1:c.200C>A	XP_011519817.1:p.Ala67Asp
XM_017022136.1:c.275C>A	XP_016877625.1:p.Ala92Asp
XM_017022137.1:c.275C>A	XP_016877626.1:p.Ala92Asp
XM_017022138.1:c.275C>A	XP_016877627.1:p.Ala92Asp
XM_017022139.1:c.-164C>A	XP_016877628.1:n.-164C>A
NM_000875.5:c.200C>A MANE Select	NP_000866.1:p.Ala67Asp
NM_001291858.2:c.200C>A	NP_001278787.1:p.Ala67Asp