Canonical Allele Identifier: CA393658873

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99478581A>G (hg19) ; chr15:g.98935352A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98935352A>G , CM000677.2:g.98935352A>G	GRCh38
NC_000015.9:g.99478581A>G , CM000677.1:g.99478581A>G	GRCh37
NC_000015.8:g.97296104A>G	NCBI36
NG_009492.1:g.290821A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3220A>G	ENSP00000496919.1:p.Thr1074Ala
ENST00000650285.1:c.3223A>G MANE Select	ENSP00000497069.1:p.Thr1075Ala
ENST00000268035.10:c.3223A>G	ENSP00000268035.6:p.Thr1075Ala
ENST00000558762.5:c.3220A>G	ENSP00000453007.1:p.Thr1074Ala
ENST00000560972.1:c.296A>G	ENSP00000453180.1:p.Asn99Ser
NM_000875.4:c.3223A>G	NP_000866.1:p.Thr1075Ala
NM_001291858.1:c.3220A>G	NP_001278787.1:p.Thr1074Ala
XM_011521513.1:c.3286A>G	XP_011519815.1:p.Thr1096Ala
XM_011521514.1:c.3286A>G	XP_011519816.1:p.Thr1096Ala
XM_011521515.1:c.3283A>G	XP_011519817.1:p.Thr1095Ala
XM_011521516.1:c.2314A>G	XP_011519818.1:p.Thr772Ala
XM_011521517.1:c.1888A>G	XP_011519819.1:p.Thr630Ala
XM_011521516.2:c.2314A>G	XP_011519818.1:p.Thr772Ala
XM_011521517.2:c.1888A>G	XP_011519819.1:p.Thr630Ala
XM_017022136.1:c.3298A>G	XP_016877625.1:p.Thr1100Ala
XM_017022137.1:c.3298A>G	XP_016877626.1:p.Thr1100Ala
XM_017022138.1:c.3295A>G	XP_016877627.1:p.Thr1099Ala
XM_017022139.1:c.2860A>G	XP_016877628.1:p.Thr954Ala
XM_024449913.1:c.2314A>G	XP_024305681.1:p.Thr772Ala
NM_000875.5:c.3223A>G MANE Select	NP_000866.1:p.Thr1075Ala
NM_001291858.2:c.3220A>G	NP_001278787.1:p.Thr1074Ala