Canonical Allele Identifier: CA492686318

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99251083G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707854G>C , CM000677.2:g.98707854G>C	GRCh38
NC_000015.9:g.99251083G>C , CM000677.1:g.99251083G>C	GRCh37
NC_000015.8:g.97068606G>C	NCBI36
NG_009492.1:g.63323G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.387G>C	ENSP00000496919.1:p.Gly129=
ENST00000650285.1:c.387G>C MANE Select	ENSP00000497069.1:p.Gly129=
ENST00000268035.10:c.387G>C	ENSP00000268035.6:p.Gly129=
ENST00000558355.1:c.24G>C	ENSP00000453630.1:p.Gly8=
ENST00000558762.5:c.387G>C	ENSP00000453007.1:p.Gly129=
ENST00000559925.5:n.387G>C
NM_000875.4:c.387G>C	NP_000866.1:p.Gly129=
NM_001291858.1:c.387G>C	NP_001278787.1:p.Gly129=
XM_011521513.1:c.387G>C	XP_011519815.1:p.Gly129=
XM_011521514.1:c.387G>C	XP_011519816.1:p.Gly129=
XM_011521515.1:c.387G>C	XP_011519817.1:p.Gly129=
XM_017022136.1:c.462G>C	XP_016877625.1:p.Gly154=
XM_017022137.1:c.462G>C	XP_016877626.1:p.Gly154=
XM_017022138.1:c.462G>C	XP_016877627.1:p.Gly154=
XM_017022139.1:c.24G>C	XP_016877628.1:p.Gly8=
NM_000875.5:c.387G>C MANE Select	NP_000866.1:p.Gly129=
NM_001291858.2:c.387G>C	NP_001278787.1:p.Gly129=