Canonical Allele Identifier: CA393675654

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99452020C>G (hg19) ; chr15:g.98908791C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908791C>G , CM000677.2:g.98908791C>G	GRCh38
NC_000015.9:g.99452020C>G , CM000677.1:g.99452020C>G	GRCh37
NC_000015.8:g.97269543C>G	NCBI36
NG_009492.1:g.264260C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1354C>G	ENSP00000496919.1:p.Pro452Ala
ENST00000650285.1:c.1354C>G MANE Select	ENSP00000497069.1:p.Pro452Ala
ENST00000268035.10:c.1354C>G	ENSP00000268035.6:p.Pro452Ala
ENST00000558762.5:c.1354C>G	ENSP00000453007.1:p.Pro452Ala
ENST00000558898.1:c.445C>G	ENSP00000454115.1:p.Pro149Ala
ENST00000559582.1:n.261C>G
ENST00000559925.5:n.1354C>G
NM_000875.4:c.1354C>G	NP_000866.1:p.Pro452Ala
NM_001291858.1:c.1354C>G	NP_001278787.1:p.Pro452Ala
XM_011521513.1:c.1417C>G	XP_011519815.1:p.Pro473Ala
XM_011521514.1:c.1417C>G	XP_011519816.1:p.Pro473Ala
XM_011521515.1:c.1417C>G	XP_011519817.1:p.Pro473Ala
XM_011521516.1:c.445C>G	XP_011519818.1:p.Pro149Ala
XM_011521517.1:c.19C>G	XP_011519819.1:p.Pro7Ala
XM_011521516.2:c.445C>G	XP_011519818.1:p.Pro149Ala
XM_011521517.2:c.19C>G	XP_011519819.1:p.Pro7Ala
XM_017022136.1:c.1429C>G	XP_016877625.1:p.Pro477Ala
XM_017022137.1:c.1429C>G	XP_016877626.1:p.Pro477Ala
XM_017022138.1:c.1429C>G	XP_016877627.1:p.Pro477Ala
XM_017022139.1:c.991C>G	XP_016877628.1:p.Pro331Ala
XM_024449913.1:c.445C>G	XP_024305681.1:p.Pro149Ala
NM_000875.5:c.1354C>G MANE Select	NP_000866.1:p.Pro452Ala
NM_001291858.2:c.1354C>G	NP_001278787.1:p.Pro452Ala