Canonical Allele Identifier: CA492686200

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99250963A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707734A>C , CM000677.2:g.98707734A>C	GRCh38
NC_000015.9:g.99250963A>C , CM000677.1:g.99250963A>C	GRCh37
NC_000015.8:g.97068486A>C	NCBI36
NG_009492.1:g.63203A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000649865.1:c.267A>C	ENSP00000496919.1:p.Arg89=
ENST00000650285.1:c.267A>C MANE Select	ENSP00000497069.1:p.Arg89=
ENST00000268035.10:c.267A>C	ENSP00000268035.6:p.Arg89=
ENST00000558762.5:c.267A>C	ENSP00000453007.1:p.Arg89=
ENST00000559925.5:n.267A>C
NM_000875.4:c.267A>C	NP_000866.1:p.Arg89=
NM_001291858.1:c.267A>C	NP_001278787.1:p.Arg89=
XM_011521513.1:c.267A>C	XP_011519815.1:p.Arg89=
XM_011521514.1:c.267A>C	XP_011519816.1:p.Arg89=
XM_011521515.1:c.267A>C	XP_011519817.1:p.Arg89=
XM_017022136.1:c.342A>C	XP_016877625.1:p.Arg114=
XM_017022137.1:c.342A>C	XP_016877626.1:p.Arg114=
XM_017022138.1:c.342A>C	XP_016877627.1:p.Arg114=
XM_017022139.1:c.-97A>C	XP_016877628.1:n.-97A>C
NM_000875.5:c.267A>C MANE Select	NP_000866.1:p.Arg89=
NM_001291858.2:c.267A>C	NP_001278787.1:p.Arg89=