Canonical Allele Identifier: CA2199287622
Gene: IGF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98913054A= , CM000677.2:g.98913054A= GRCh38
NC_000015.9:g.99456283A= , CM000677.1:g.99456283A= GRCh37
NC_000015.8:g.97273806A= NCBI36
NG_009492.1:g.268523A=

Transcript Alleles

HGVS Amino-acid change
ENST00000649865.1:c.1600A= ENSP00000496919.1:p.Asn534=
ENST00000650285.1:c.1600A= MANE Select ENSP00000497069.1:p.Asn534=
ENST00000268035.10:c.1600A= ENSP00000268035.6:p.Asn534=
ENST00000558762.5:c.1600A= ENSP00000453007.1:p.Asn534=
ENST00000559582.1:n.507A=
ENST00000559925.5:n.1600A=
NM_000875.4:c.1600A= NP_000866.1:p.Asn534=
NM_001291858.1:c.1600A= NP_001278787.1:p.Asn534=
XM_011521513.1:c.1663A= XP_011519815.1:p.Asn555=
XM_011521514.1:c.1663A= XP_011519816.1:p.Asn555=
XM_011521515.1:c.1663A= XP_011519817.1:p.Asn555=
XM_011521516.1:c.691A= XP_011519818.1:p.Asn231=
XM_011521517.1:c.265A= XP_011519819.1:p.Asn89=
XM_011521516.2:c.691A= XP_011519818.1:p.Asn231=
XM_011521517.2:c.265A= XP_011519819.1:p.Asn89=
XM_017022136.1:c.1675A= XP_016877625.1:p.Asn559=
XM_017022137.1:c.1675A= XP_016877626.1:p.Asn559=
XM_017022138.1:c.1675A= XP_016877627.1:p.Asn559=
XM_017022139.1:c.1237A= XP_016877628.1:p.Asn413=
XM_024449913.1:c.691A= XP_024305681.1:p.Asn231=
NM_000875.5:c.1600A= MANE Select NP_000866.1:p.Asn534=
NM_001291858.2:c.1600A= NP_001278787.1:p.Asn534=