Canonical Allele Identifier: CA14113018

Gene: IGF1R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98949084C>T , CM000677.2:g.98949084C>T	GRCh38
NC_000015.9:g.99492313C>T , CM000677.1:g.99492313C>T	GRCh37
NC_000015.8:g.97309836C>T	NCBI36
NG_009492.1:g.304553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3719+376C>T	ENSP00000496919.1:n.3719+376C>T
ENST00000650285.1:c.3722+376C>T MANE Select	ENSP00000497069.1:n.3722+376C>T
ENST00000268035.10:c.3722+376C>T	ENSP00000268035.6:n.3722+376C>T
ENST00000558762.5:c.3719+376C>T	ENSP00000453007.1:n.3719+376C>T
NM_000875.4:c.3722+376C>T	NP_000866.1:n.3722+376C>T
NM_001291858.1:c.3719+376C>T	NP_001278787.1:n.3719+376C>T
XM_011521513.1:c.3785+376C>T	XP_011519815.1:n.3785+376C>T
XM_011521514.1:c.3785+376C>T	XP_011519816.1:n.3785+376C>T
XM_011521515.1:c.3782+376C>T	XP_011519817.1:n.3782+376C>T
XM_011521516.1:c.2813+376C>T	XP_011519818.1:n.2813+376C>T
XM_011521517.1:c.2387+376C>T	XP_011519819.1:n.2387+376C>T
XM_011521516.2:c.2813+376C>T	XP_011519818.1:n.2813+376C>T
XM_011521517.2:c.2387+376C>T	XP_011519819.1:n.2387+376C>T
XM_017022136.1:c.3797+376C>T	XP_016877625.1:n.3797+376C>T
XM_017022137.1:c.3797+376C>T	XP_016877626.1:n.3797+376C>T
XM_017022138.1:c.3794+376C>T	XP_016877627.1:n.3794+376C>T
XM_017022139.1:c.3359+376C>T	XP_016877628.1:n.3359+376C>T
XM_024449913.1:c.2813+376C>T	XP_024305681.1:n.2813+376C>T
NM_000875.5:c.3722+376C>T MANE Select	NP_000866.1:n.3722+376C>T
NM_001291858.2:c.3719+376C>T	NP_001278787.1:n.3719+376C>T