Canonical Allele Identifier: CA2199275058

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98935344G= , CM000677.2:g.98935344G=	GRCh38
NC_000015.9:g.99478573G= , CM000677.1:g.99478573G=	GRCh37
NC_000015.8:g.97296096G=	NCBI36
NG_009492.1:g.290813G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3212G=	ENSP00000496919.1:p.Gly1071=
ENST00000650285.1:c.3215G= MANE Select	ENSP00000497069.1:p.Gly1072=
ENST00000268035.10:c.3215G=	ENSP00000268035.6:p.Gly1072=
ENST00000558762.5:c.3212G=	ENSP00000453007.1:p.Gly1071=
ENST00000560972.1:c.288G=	ENSP00000453180.1:p.Arg96=
NM_000875.4:c.3215G=	NP_000866.1:p.Gly1072=
NM_001291858.1:c.3212G=	NP_001278787.1:p.Gly1071=
XM_011521513.1:c.3278G=	XP_011519815.1:p.Gly1093=
XM_011521514.1:c.3278G=	XP_011519816.1:p.Gly1093=
XM_011521515.1:c.3275G=	XP_011519817.1:p.Gly1092=
XM_011521516.1:c.2306G=	XP_011519818.1:p.Gly769=
XM_011521517.1:c.1880G=	XP_011519819.1:p.Gly627=
XM_011521516.2:c.2306G=	XP_011519818.1:p.Gly769=
XM_011521517.2:c.1880G=	XP_011519819.1:p.Gly627=
XM_017022136.1:c.3290G=	XP_016877625.1:p.Gly1097=
XM_017022137.1:c.3290G=	XP_016877626.1:p.Gly1097=
XM_017022138.1:c.3287G=	XP_016877627.1:p.Gly1096=
XM_017022139.1:c.2852G=	XP_016877628.1:p.Gly951=
XM_024449913.1:c.2306G=	XP_024305681.1:p.Gly769=
NM_000875.5:c.3215G= MANE Select	NP_000866.1:p.Gly1072=
NM_001291858.2:c.3212G=	NP_001278787.1:p.Gly1071=