Canonical Allele Identifier: CA7752067

Gene: IGF1R

Linked Data

• dbSNP Id: rs751361664
• ExAC: 15:99451941 C / T
• gnomAD v2: 15-99451941-C-T
• gnomAD v3: 15-98908712-C-T
• gnomAD v4: 15-98908712-C-T
• MyVariant Identifiers: chr15:g.99451941C>T (hg19) ; chr15:g.98908712C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908712C>T , CM000677.2:g.98908712C>T	GRCh38
NC_000015.9:g.99451941C>T , CM000677.1:g.99451941C>T	GRCh37
NC_000015.8:g.97269464C>T	NCBI36
NG_009492.1:g.264181C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1275C>T	ENSP00000496919.1:p.Asn425=
ENST00000650285.1:c.1275C>T MANE Select	ENSP00000497069.1:p.Asn425=
ENST00000268035.10:c.1275C>T	ENSP00000268035.6:p.Asn425=
ENST00000558762.5:c.1275C>T	ENSP00000453007.1:p.Asn425=
ENST00000558898.1:c.366C>T	ENSP00000454115.1:p.Asn122=
ENST00000559582.1:n.182C>T
ENST00000559925.5:n.1275C>T
NM_000875.4:c.1275C>T	NP_000866.1:p.Asn425=
NM_001291858.1:c.1275C>T	NP_001278787.1:p.Asn425=
XM_011521513.1:c.1338C>T	XP_011519815.1:p.Asn446=
XM_011521514.1:c.1338C>T	XP_011519816.1:p.Asn446=
XM_011521515.1:c.1338C>T	XP_011519817.1:p.Asn446=
XM_011521516.1:c.366C>T	XP_011519818.1:p.Asn122=
XM_011521517.1:c.-61C>T	XP_011519819.1:n.-61C>T
XM_011521516.2:c.366C>T	XP_011519818.1:p.Asn122=
XM_011521517.2:c.-61C>T	XP_011519819.1:n.-61C>T
XM_017022136.1:c.1350C>T	XP_016877625.1:p.Asn450=
XM_017022137.1:c.1350C>T	XP_016877626.1:p.Asn450=
XM_017022138.1:c.1350C>T	XP_016877627.1:p.Asn450=
XM_017022139.1:c.912C>T	XP_016877628.1:p.Asn304=
XM_024449913.1:c.366C>T	XP_024305681.1:p.Asn122=
NM_000875.5:c.1275C>T MANE Select	NP_000866.1:p.Asn425=
NM_001291858.2:c.1275C>T	NP_001278787.1:p.Asn425=