Canonical Allele Identifier: CA393658743

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99478552T>G (hg19) ; chr15:g.98935323T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98935323T>G , CM000677.2:g.98935323T>G	GRCh38
NC_000015.9:g.99478552T>G , CM000677.1:g.99478552T>G	GRCh37
NC_000015.8:g.97296075T>G	NCBI36
NG_009492.1:g.290792T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3191T>G	ENSP00000496919.1:p.Leu1064Trp
ENST00000650285.1:c.3194T>G MANE Select	ENSP00000497069.1:p.Leu1065Trp
ENST00000268035.10:c.3194T>G	ENSP00000268035.6:p.Leu1065Trp
ENST00000558762.5:c.3191T>G	ENSP00000453007.1:p.Leu1064Trp
ENST00000560972.1:c.267T>G	ENSP00000453180.1:p.Ile89Met
NM_000875.4:c.3194T>G	NP_000866.1:p.Leu1065Trp
NM_001291858.1:c.3191T>G	NP_001278787.1:p.Leu1064Trp
XM_011521513.1:c.3257T>G	XP_011519815.1:p.Leu1086Trp
XM_011521514.1:c.3257T>G	XP_011519816.1:p.Leu1086Trp
XM_011521515.1:c.3254T>G	XP_011519817.1:p.Leu1085Trp
XM_011521516.1:c.2285T>G	XP_011519818.1:p.Leu762Trp
XM_011521517.1:c.1859T>G	XP_011519819.1:p.Leu620Trp
XM_011521516.2:c.2285T>G	XP_011519818.1:p.Leu762Trp
XM_011521517.2:c.1859T>G	XP_011519819.1:p.Leu620Trp
XM_017022136.1:c.3269T>G	XP_016877625.1:p.Leu1090Trp
XM_017022137.1:c.3269T>G	XP_016877626.1:p.Leu1090Trp
XM_017022138.1:c.3266T>G	XP_016877627.1:p.Leu1089Trp
XM_017022139.1:c.2831T>G	XP_016877628.1:p.Leu944Trp
XM_024449913.1:c.2285T>G	XP_024305681.1:p.Leu762Trp
NM_000875.5:c.3194T>G MANE Select	NP_000866.1:p.Leu1065Trp
NM_001291858.2:c.3191T>G	NP_001278787.1:p.Leu1064Trp