Canonical Allele Identifier: CA492324912
Gene: IGF1R HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.99452091G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98908862G>A , CM000677.2:g.98908862G>A GRCh38
NC_000015.9:g.99452091G>A , CM000677.1:g.99452091G>A GRCh37
NC_000015.8:g.97269614G>A NCBI36
NG_009492.1:g.264331G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.1425G>A ENSP00000496919.1:p.Gly475=
ENST00000650285.1:c.1425G>A MANE Select ENSP00000497069.1:p.Gly475=
ENST00000268035.10:c.1425G>A ENSP00000268035.6:p.Gly475=
ENST00000558762.5:c.1425G>A ENSP00000453007.1:p.Gly475=
ENST00000558898.1:c.516G>A ENSP00000454115.1:p.Gly172=
ENST00000559582.1:n.332G>A
ENST00000559925.5:n.1425G>A
NM_000875.4:c.1425G>A NP_000866.1:p.Gly475=
NM_001291858.1:c.1425G>A NP_001278787.1:p.Gly475=
XM_011521513.1:c.1488G>A XP_011519815.1:p.Gly496=
XM_011521514.1:c.1488G>A XP_011519816.1:p.Gly496=
XM_011521515.1:c.1488G>A XP_011519817.1:p.Gly496=
XM_011521516.1:c.516G>A XP_011519818.1:p.Gly172=
XM_011521517.1:c.90G>A XP_011519819.1:p.Gly30=
XM_011521516.2:c.516G>A XP_011519818.1:p.Gly172=
XM_011521517.2:c.90G>A XP_011519819.1:p.Gly30=
XM_017022136.1:c.1500G>A XP_016877625.1:p.Gly500=
XM_017022137.1:c.1500G>A XP_016877626.1:p.Gly500=
XM_017022138.1:c.1500G>A XP_016877627.1:p.Gly500=
XM_017022139.1:c.1062G>A XP_016877628.1:p.Gly354=
XM_024449913.1:c.516G>A XP_024305681.1:p.Gly172=
NM_000875.5:c.1425G>A MANE Select NP_000866.1:p.Gly475=
NM_001291858.2:c.1425G>A NP_001278787.1:p.Gly475=