Canonical Allele Identifier: CA393676332

Gene: IGF1R

Linked Data

• dbSNP Id: rs2014857301
• gnomAD v3: 15-98908866-A-G
• gnomAD v4: 15-98908866-A-G
• MyVariant Identifiers: chr15:g.99452095A>G (hg19) ; chr15:g.98908866A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908866A>G , CM000677.2:g.98908866A>G	GRCh38
NC_000015.9:g.99452095A>G , CM000677.1:g.99452095A>G	GRCh37
NC_000015.8:g.97269618A>G	NCBI36
NG_009492.1:g.264335A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1429A>G	ENSP00000496919.1:p.Ile477Val
ENST00000650285.1:c.1429A>G MANE Select	ENSP00000497069.1:p.Ile477Val
ENST00000268035.10:c.1429A>G	ENSP00000268035.6:p.Ile477Val
ENST00000558762.5:c.1429A>G	ENSP00000453007.1:p.Ile477Val
ENST00000558898.1:c.520A>G	ENSP00000454115.1:p.Ile174Val
ENST00000559582.1:n.336A>G
ENST00000559925.5:n.1429A>G
NM_000875.4:c.1429A>G	NP_000866.1:p.Ile477Val
NM_001291858.1:c.1429A>G	NP_001278787.1:p.Ile477Val
XM_011521513.1:c.1492A>G	XP_011519815.1:p.Ile498Val
XM_011521514.1:c.1492A>G	XP_011519816.1:p.Ile498Val
XM_011521515.1:c.1492A>G	XP_011519817.1:p.Ile498Val
XM_011521516.1:c.520A>G	XP_011519818.1:p.Ile174Val
XM_011521517.1:c.94A>G	XP_011519819.1:p.Ile32Val
XM_011521516.2:c.520A>G	XP_011519818.1:p.Ile174Val
XM_011521517.2:c.94A>G	XP_011519819.1:p.Ile32Val
XM_017022136.1:c.1504A>G	XP_016877625.1:p.Ile502Val
XM_017022137.1:c.1504A>G	XP_016877626.1:p.Ile502Val
XM_017022138.1:c.1504A>G	XP_016877627.1:p.Ile502Val
XM_017022139.1:c.1066A>G	XP_016877628.1:p.Ile356Val
XM_024449913.1:c.520A>G	XP_024305681.1:p.Ile174Val
NM_000875.5:c.1429A>G MANE Select	NP_000866.1:p.Ile477Val
NM_001291858.2:c.1429A>G	NP_001278787.1:p.Ile477Val