Canonical Allele Identifier: CA275819396

Gene: IGF1R

Linked Data

• dbSNP Id: rs375153085
• MyVariant Identifiers: chr15:g.99251015C>T (hg19) ; chr15:g.98707786C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707786C>T , CM000677.2:g.98707786C>T	GRCh38
NC_000015.9:g.99251015C>T , CM000677.1:g.99251015C>T	GRCh37
NC_000015.8:g.97068538C>T	NCBI36
NG_009492.1:g.63255C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649865.1:c.319C>T	ENSP00000496919.1:p.Arg107Cys
ENST00000650285.1:c.319C>T MANE Select	ENSP00000497069.1:p.Arg107Cys
ENST00000268035.10:c.319C>T	ENSP00000268035.6:p.Arg107Cys
ENST00000558762.5:c.319C>T	ENSP00000453007.1:p.Arg107Cys
ENST00000559925.5:n.319C>T
NM_000875.4:c.319C>T	NP_000866.1:p.Arg107Cys
NM_001291858.1:c.319C>T	NP_001278787.1:p.Arg107Cys
XM_011521513.1:c.319C>T	XP_011519815.1:p.Arg107Cys
XM_011521514.1:c.319C>T	XP_011519816.1:p.Arg107Cys
XM_011521515.1:c.319C>T	XP_011519817.1:p.Arg107Cys
XM_017022136.1:c.394C>T	XP_016877625.1:p.Arg132Cys
XM_017022137.1:c.394C>T	XP_016877626.1:p.Arg132Cys
XM_017022138.1:c.394C>T	XP_016877627.1:p.Arg132Cys
XM_017022139.1:c.-45C>T	XP_016877628.1:n.-45C>T
NM_000875.5:c.319C>T MANE Select	NP_000866.1:p.Arg107Cys
NM_001291858.2:c.319C>T	NP_001278787.1:p.Arg107Cys