Canonical Allele Identifier: CA2199299344

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98960571G= , CM000677.2:g.98960571G=	GRCh38
NC_000015.9:g.99503800G= , CM000677.1:g.99503800G=	GRCh37
NC_000015.8:g.97321323G=	NCBI36
NG_009492.1:g.316040G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000875.5:c.*3129G= MANE Select	NP_000866.1:n.*3129G=
ENST00000650285.1:c.*3129G= MANE Select	ENSP00000497069.1:n.*3129G=
NM_000875.4:c.*3129G=	NP_000866.1:n.*3129G=
NM_001291858.1:c.*3129G=	NP_001278787.1:n.*3129G=
NM_001291858.2:c.*3129G=	NP_001278787.1:n.*3129G=
ENST00000268035.10:c.*3129G=	ENSP00000268035.6:n.*3129G=
ENST00000558762.5:c.*3129G=	ENSP00000453007.1:n.*3129G=
ENST00000649865.1:c.*3129G=	ENSP00000496919.1:n.*3129G=
XM_011521513.1:c.*3129G=	XP_011519815.1:n.*3129G=
XM_011521514.1:c.*2643G=	XP_011519816.1:n.*2643G=
XM_011521515.1:c.*3129G=	XP_011519817.1:n.*3129G=
XM_011521516.1:c.*3129G=	XP_011519818.1:n.*3129G=
XM_011521517.1:c.*3129G=	XP_011519819.1:n.*3129G=
XM_017022136.1:c.*3129G=	XP_016877625.1:n.*3129G=
XM_017022137.1:c.*2643G=	XP_016877626.1:n.*2643G=
XM_017022138.1:c.*3129G=	XP_016877627.1:n.*3129G=