Canonical Allele Identifier: CA492682370
Gene: IGF1R HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.99456273A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98913044A>T , CM000677.2:g.98913044A>T GRCh38
NC_000015.9:g.99456273A>T , CM000677.1:g.99456273A>T GRCh37
NC_000015.8:g.97273796A>T NCBI36
NG_009492.1:g.268513A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649865.1:c.1590A>T ENSP00000496919.1:p.Ala530=
ENST00000650285.1:c.1590A>T MANE Select ENSP00000497069.1:p.Ala530=
ENST00000268035.10:c.1590A>T ENSP00000268035.6:p.Ala530=
ENST00000558762.5:c.1590A>T ENSP00000453007.1:p.Ala530=
ENST00000559582.1:n.497A>T
ENST00000559925.5:n.1590A>T
NM_000875.4:c.1590A>T NP_000866.1:p.Ala530=
NM_001291858.1:c.1590A>T NP_001278787.1:p.Ala530=
XM_011521513.1:c.1653A>T XP_011519815.1:p.Ala551=
XM_011521514.1:c.1653A>T XP_011519816.1:p.Ala551=
XM_011521515.1:c.1653A>T XP_011519817.1:p.Ala551=
XM_011521516.1:c.681A>T XP_011519818.1:p.Ala227=
XM_011521517.1:c.255A>T XP_011519819.1:p.Ala85=
XM_011521516.2:c.681A>T XP_011519818.1:p.Ala227=
XM_011521517.2:c.255A>T XP_011519819.1:p.Ala85=
XM_017022136.1:c.1665A>T XP_016877625.1:p.Ala555=
XM_017022137.1:c.1665A>T XP_016877626.1:p.Ala555=
XM_017022138.1:c.1665A>T XP_016877627.1:p.Ala555=
XM_017022139.1:c.1227A>T XP_016877628.1:p.Ala409=
XM_024449913.1:c.681A>T XP_024305681.1:p.Ala227=
NM_000875.5:c.1590A>T MANE Select NP_000866.1:p.Ala530=
NM_001291858.2:c.1590A>T NP_001278787.1:p.Ala530=