Canonical Allele Identifier: CA492306687

Gene: IGF1R

Linked Data

• gnomAD v4: 15-98935384-C-A
• MyVariant Identifiers: chr15:g.99478613C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98935384C>A , CM000677.2:g.98935384C>A	GRCh38
NC_000015.9:g.99478613C>A , CM000677.1:g.99478613C>A	GRCh37
NC_000015.8:g.97296136C>A	NCBI36
NG_009492.1:g.290853C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3252C>A	ENSP00000496919.1:p.Gly1084=
ENST00000650285.1:c.3255C>A MANE Select	ENSP00000497069.1:p.Gly1085=
ENST00000268035.10:c.3255C>A	ENSP00000268035.6:p.Gly1085=
ENST00000558762.5:c.3252C>A	ENSP00000453007.1:p.Gly1084=
NM_000875.4:c.3255C>A	NP_000866.1:p.Gly1085=
NM_001291858.1:c.3252C>A	NP_001278787.1:p.Gly1084=
XM_011521513.1:c.3318C>A	XP_011519815.1:p.Gly1106=
XM_011521514.1:c.3318C>A	XP_011519816.1:p.Gly1106=
XM_011521515.1:c.3315C>A	XP_011519817.1:p.Gly1105=
XM_011521516.1:c.2346C>A	XP_011519818.1:p.Gly782=
XM_011521517.1:c.1920C>A	XP_011519819.1:p.Gly640=
XM_011521516.2:c.2346C>A	XP_011519818.1:p.Gly782=
XM_011521517.2:c.1920C>A	XP_011519819.1:p.Gly640=
XM_017022136.1:c.3330C>A	XP_016877625.1:p.Gly1110=
XM_017022137.1:c.3330C>A	XP_016877626.1:p.Gly1110=
XM_017022138.1:c.3327C>A	XP_016877627.1:p.Gly1109=
XM_017022139.1:c.2892C>A	XP_016877628.1:p.Gly964=
XM_024449913.1:c.2346C>A	XP_024305681.1:p.Gly782=
NM_000875.5:c.3255C>A MANE Select	NP_000866.1:p.Gly1085=
NM_001291858.2:c.3252C>A	NP_001278787.1:p.Gly1084=