Canonical Allele Identifier: CA2199275059

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98935348G= , CM000677.2:g.98935348G=	GRCh38
NC_000015.9:g.99478577G= , CM000677.1:g.99478577G=	GRCh37
NC_000015.8:g.97296100G=	NCBI36
NG_009492.1:g.290817G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3216G=	ENSP00000496919.1:p.Gln1072=
ENST00000650285.1:c.3219G= MANE Select	ENSP00000497069.1:p.Gln1073=
ENST00000268035.10:c.3219G=	ENSP00000268035.6:p.Gln1073=
ENST00000558762.5:c.3216G=	ENSP00000453007.1:p.Gln1072=
ENST00000560972.1:c.292G=	ENSP00000453180.1:p.Ala98=
NM_000875.4:c.3219G=	NP_000866.1:p.Gln1073=
NM_001291858.1:c.3216G=	NP_001278787.1:p.Gln1072=
XM_011521513.1:c.3282G=	XP_011519815.1:p.Gln1094=
XM_011521514.1:c.3282G=	XP_011519816.1:p.Gln1094=
XM_011521515.1:c.3279G=	XP_011519817.1:p.Gln1093=
XM_011521516.1:c.2310G=	XP_011519818.1:p.Gln770=
XM_011521517.1:c.1884G=	XP_011519819.1:p.Gln628=
XM_011521516.2:c.2310G=	XP_011519818.1:p.Gln770=
XM_011521517.2:c.1884G=	XP_011519819.1:p.Gln628=
XM_017022136.1:c.3294G=	XP_016877625.1:p.Gln1098=
XM_017022137.1:c.3294G=	XP_016877626.1:p.Gln1098=
XM_017022138.1:c.3291G=	XP_016877627.1:p.Gln1097=
XM_017022139.1:c.2856G=	XP_016877628.1:p.Gln952=
XM_024449913.1:c.2310G=	XP_024305681.1:p.Gln770=
NM_000875.5:c.3219G= MANE Select	NP_000866.1:p.Gln1073=
NM_001291858.2:c.3216G=	NP_001278787.1:p.Gln1072=