Canonical Allele Identifier: CA7751741

Gene: IGF1R

Linked Data

• ClinVar Variation Id: 1909186
• ClinVar RCV Id: RCV002584640
• dbSNP Id: rs780029944
• ExAC: 15:99250779 G / GTC
• gnomAD v2: 15-99250779-G-GTC
• gnomAD v3: 15-98707550-G-GTC
• gnomAD v4: 15-98707550-G-GTC
• MyVariant Identifiers: chr15:g.99250779_99250780insTC (hg19) ; chr15:g.98707550_98707551insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707553_98707554dup , CM000677.2:g.98707553_98707554dup	GRCh38
NC_000015.9:g.99250782_99250783dup , CM000677.1:g.99250782_99250783dup	GRCh37
NC_000015.8:g.97068305_97068306dup	NCBI36
NG_009492.1:g.63022_63023dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.95-9_95-8dup	ENSP00000496919.1:n.95-9_95-8dup
ENST00000650285.1:c.95-9_95-8dup MANE Select	ENSP00000497069.1:n.95-9_95-8dup
ENST00000268035.10:c.95-9_95-8dup	ENSP00000268035.6:n.95-9_95-8dup
ENST00000558762.5:c.95-9_95-8dup	ENSP00000453007.1:n.95-9_95-8dup
ENST00000559925.5:n.95-9_95-8dup
NM_000875.4:c.95-9_95-8dup	NP_000866.1:n.95-9_95-8dup
NM_001291858.1:c.95-9_95-8dup	NP_001278787.1:n.95-9_95-8dup
XM_011521513.1:c.95-9_95-8dup	XP_011519815.1:n.95-9_95-8dup
XM_011521514.1:c.95-9_95-8dup	XP_011519816.1:n.95-9_95-8dup
XM_011521515.1:c.95-9_95-8dup	XP_011519817.1:n.95-9_95-8dup
XM_017022136.1:c.170-9_170-8dup	XP_016877625.1:n.170-9_170-8dup
XM_017022137.1:c.170-9_170-8dup	XP_016877626.1:n.170-9_170-8dup
XM_017022138.1:c.170-9_170-8dup	XP_016877627.1:n.170-9_170-8dup
XM_017022139.1:c.-269-9_-269-8dup	XP_016877628.1:n.-269-9_-269-8dup
NM_000875.5:c.95-9_95-8dup MANE Select	NP_000866.1:n.95-9_95-8dup
NM_001291858.2:c.95-9_95-8dup	NP_001278787.1:n.95-9_95-8dup