Canonical Allele Identifier: CA393658798

Gene: IGF1R

Linked Data

• MyVariant Identifiers: chr15:g.99478565G>C (hg19) ; chr15:g.98935336G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98935336G>C , CM000677.2:g.98935336G>C	GRCh38
NC_000015.9:g.99478565G>C , CM000677.1:g.99478565G>C	GRCh37
NC_000015.8:g.97296088G>C	NCBI36
NG_009492.1:g.290805G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3204G>C	ENSP00000496919.1:p.Val1068=
ENST00000650285.1:c.3207G>C MANE Select	ENSP00000497069.1:p.Val1069=
ENST00000268035.10:c.3207G>C	ENSP00000268035.6:p.Val1069=
ENST00000558762.5:c.3204G>C	ENSP00000453007.1:p.Val1068=
ENST00000560972.1:c.280G>C	ENSP00000453180.1:p.Val94Leu
NM_000875.4:c.3207G>C	NP_000866.1:p.Val1069=
NM_001291858.1:c.3204G>C	NP_001278787.1:p.Val1068=
XM_011521513.1:c.3270G>C	XP_011519815.1:p.Val1090=
XM_011521514.1:c.3270G>C	XP_011519816.1:p.Val1090=
XM_011521515.1:c.3267G>C	XP_011519817.1:p.Val1089=
XM_011521516.1:c.2298G>C	XP_011519818.1:p.Val766=
XM_011521517.1:c.1872G>C	XP_011519819.1:p.Val624=
XM_011521516.2:c.2298G>C	XP_011519818.1:p.Val766=
XM_011521517.2:c.1872G>C	XP_011519819.1:p.Val624=
XM_017022136.1:c.3282G>C	XP_016877625.1:p.Val1094=
XM_017022137.1:c.3282G>C	XP_016877626.1:p.Val1094=
XM_017022138.1:c.3279G>C	XP_016877627.1:p.Val1093=
XM_017022139.1:c.2844G>C	XP_016877628.1:p.Val948=
XM_024449913.1:c.2298G>C	XP_024305681.1:p.Val766=
NM_000875.5:c.3207G>C MANE Select	NP_000866.1:p.Val1069=
NM_001291858.2:c.3204G>C	NP_001278787.1:p.Val1068=