Canonical Allele Identifier: CA492306777
Gene: IGF1R HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.99478640G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98935411G>T , CM000677.2:g.98935411G>T GRCh38
NC_000015.9:g.99478640G>T , CM000677.1:g.99478640G>T GRCh37
NC_000015.8:g.97296163G>T NCBI36
NG_009492.1:g.290880G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.3279G>T ENSP00000496919.1:p.Leu1093=
ENST00000650285.1:c.3282G>T MANE Select ENSP00000497069.1:p.Leu1094=
ENST00000268035.10:c.3282G>T ENSP00000268035.6:p.Leu1094=
ENST00000558762.5:c.3279G>T ENSP00000453007.1:p.Leu1093=
NM_000875.4:c.3282G>T NP_000866.1:p.Leu1094=
NM_001291858.1:c.3279G>T NP_001278787.1:p.Leu1093=
XM_011521513.1:c.3345G>T XP_011519815.1:p.Leu1115=
XM_011521514.1:c.3345G>T XP_011519816.1:p.Leu1115=
XM_011521515.1:c.3342G>T XP_011519817.1:p.Leu1114=
XM_011521516.1:c.2373G>T XP_011519818.1:p.Leu791=
XM_011521517.1:c.1947G>T XP_011519819.1:p.Leu649=
XM_011521516.2:c.2373G>T XP_011519818.1:p.Leu791=
XM_011521517.2:c.1947G>T XP_011519819.1:p.Leu649=
XM_017022136.1:c.3357G>T XP_016877625.1:p.Leu1119=
XM_017022137.1:c.3357G>T XP_016877626.1:p.Leu1119=
XM_017022138.1:c.3354G>T XP_016877627.1:p.Leu1118=
XM_017022139.1:c.2919G>T XP_016877628.1:p.Leu973=
XM_024449913.1:c.2373G>T XP_024305681.1:p.Leu791=
NM_000875.5:c.3282G>T MANE Select NP_000866.1:p.Leu1094=
NM_001291858.2:c.3279G>T NP_001278787.1:p.Leu1093=