Canonical Allele Identifier: CA393674477

Gene: IGF1R

Linked Data

• gnomAD v4: 15-98908684-G-C
• MyVariant Identifiers: chr15:g.99451913G>C (hg19) ; chr15:g.98908684G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908684G>C , CM000677.2:g.98908684G>C	GRCh38
NC_000015.9:g.99451913G>C , CM000677.1:g.99451913G>C	GRCh37
NC_000015.8:g.97269436G>C	NCBI36
NG_009492.1:g.264153G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000649865.1:c.1248-1G>C	ENSP00000496919.1:n.1248-1G>C
ENST00000650285.1:c.1248-1G>C MANE Select	ENSP00000497069.1:n.1248-1G>C
ENST00000268035.10:c.1248-1G>C	ENSP00000268035.6:n.1248-1G>C
ENST00000558762.5:c.1248-1G>C	ENSP00000453007.1:n.1248-1G>C
ENST00000558898.1:c.339-1G>C	ENSP00000454115.1:n.339-1G>C
ENST00000559582.1:n.155-1G>C
ENST00000559925.5:n.1248-1G>C
NM_000875.4:c.1248-1G>C	NP_000866.1:n.1248-1G>C
NM_001291858.1:c.1248-1G>C	NP_001278787.1:n.1248-1G>C
XM_011521513.1:c.1311-1G>C	XP_011519815.1:n.1311-1G>C
XM_011521514.1:c.1311-1G>C	XP_011519816.1:n.1311-1G>C
XM_011521515.1:c.1311-1G>C	XP_011519817.1:n.1311-1G>C
XM_011521516.1:c.339-1G>C	XP_011519818.1:n.339-1G>C
XM_011521517.1:c.-88-1G>C	XP_011519819.1:n.-88-1G>C
XM_011521516.2:c.339-1G>C	XP_011519818.1:n.339-1G>C
XM_011521517.2:c.-88-1G>C	XP_011519819.1:n.-88-1G>C
XM_017022136.1:c.1323-1G>C	XP_016877625.1:n.1323-1G>C
XM_017022137.1:c.1323-1G>C	XP_016877626.1:n.1323-1G>C
XM_017022138.1:c.1323-1G>C	XP_016877627.1:n.1323-1G>C
XM_017022139.1:c.885-1G>C	XP_016877628.1:n.885-1G>C
XM_024449913.1:c.339-1G>C	XP_024305681.1:n.339-1G>C
NM_000875.5:c.1248-1G>C MANE Select	NP_000866.1:n.1248-1G>C
NM_001291858.2:c.1248-1G>C	NP_001278787.1:n.1248-1G>C