Canonical Allele Identifier: CA492306668

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99478607A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98935378A>C , CM000677.2:g.98935378A>C	GRCh38
NC_000015.9:g.99478607A>C , CM000677.1:g.99478607A>C	GRCh37
NC_000015.8:g.97296130A>C	NCBI36
NG_009492.1:g.290847A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3246A>C	ENSP00000496919.1:p.Thr1082=
ENST00000650285.1:c.3249A>C MANE Select	ENSP00000497069.1:p.Thr1083=
ENST00000268035.10:c.3249A>C	ENSP00000268035.6:p.Thr1083=
ENST00000558762.5:c.3246A>C	ENSP00000453007.1:p.Thr1082=
NM_000875.4:c.3249A>C	NP_000866.1:p.Thr1083=
NM_001291858.1:c.3246A>C	NP_001278787.1:p.Thr1082=
XM_011521513.1:c.3312A>C	XP_011519815.1:p.Thr1104=
XM_011521514.1:c.3312A>C	XP_011519816.1:p.Thr1104=
XM_011521515.1:c.3309A>C	XP_011519817.1:p.Thr1103=
XM_011521516.1:c.2340A>C	XP_011519818.1:p.Thr780=
XM_011521517.1:c.1914A>C	XP_011519819.1:p.Thr638=
XM_011521516.2:c.2340A>C	XP_011519818.1:p.Thr780=
XM_011521517.2:c.1914A>C	XP_011519819.1:p.Thr638=
XM_017022136.1:c.3324A>C	XP_016877625.1:p.Thr1108=
XM_017022137.1:c.3324A>C	XP_016877626.1:p.Thr1108=
XM_017022138.1:c.3321A>C	XP_016877627.1:p.Thr1107=
XM_017022139.1:c.2886A>C	XP_016877628.1:p.Thr962=
XM_024449913.1:c.2340A>C	XP_024305681.1:p.Thr780=
NM_000875.5:c.3249A>C MANE Select	NP_000866.1:p.Thr1083=
NM_001291858.2:c.3246A>C	NP_001278787.1:p.Thr1082=