Canonical Allele Identifier: CA7752091

Gene: IGF1R

Linked Data

• dbSNP Id: rs750811818
• ExAC: 15:99452152 C / CATCATG
• gnomAD v2: 15-99452152-C-CATCATG
• gnomAD v4: 15-98908923-C-CATCATG
• MyVariant Identifiers: chr15:g.99452152_99452153insATCATG (hg19) ; chr15:g.98908923_98908924insATCATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908923_98908924insATCATG , CM000677.2:g.98908923_98908924insATCATG	GRCh38
NC_000015.9:g.99452152_99452153insATCATG , CM000677.1:g.99452152_99452153insATCATG	GRCh37
NC_000015.8:g.97269675_97269676insATCATG	NCBI36
NG_009492.1:g.264392_264393insATCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1462+24_1462+25insATCATG	ENSP00000496919.1:n.1462+24_1462+25insATCATG
ENST00000650285.1:c.1462+24_1462+25insATCATG MANE Select	ENSP00000497069.1:n.1462+24_1462+25insATCATG
ENST00000268035.10:c.1462+24_1462+25insATCATG	ENSP00000268035.6:n.1462+24_1462+25insATCATG
ENST00000558762.5:c.1462+24_1462+25insATCATG	ENSP00000453007.1:n.1462+24_1462+25insATCATG
ENST00000558898.1:c.553+24_553+25insATCATG	ENSP00000454115.1:n.553+24_553+25insATCATG
ENST00000559582.1:n.369+24_369+25insATCATG
ENST00000559925.5:n.1462+24_1462+25insATCATG
NM_000875.4:c.1462+24_1462+25insATCATG	NP_000866.1:n.1462+24_1462+25insATCATG
NM_001291858.1:c.1462+24_1462+25insATCATG	NP_001278787.1:n.1462+24_1462+25insATCATG
XM_011521513.1:c.1525+24_1525+25insATCATG	XP_011519815.1:n.1525+24_1525+25insATCATG
XM_011521514.1:c.1525+24_1525+25insATCATG	XP_011519816.1:n.1525+24_1525+25insATCATG
XM_011521515.1:c.1525+24_1525+25insATCATG	XP_011519817.1:n.1525+24_1525+25insATCATG
XM_011521516.1:c.553+24_553+25insATCATG	XP_011519818.1:n.553+24_553+25insATCATG
XM_011521517.1:c.127+24_127+25insATCATG	XP_011519819.1:n.127+24_127+25insATCATG
XM_011521516.2:c.553+24_553+25insATCATG	XP_011519818.1:n.553+24_553+25insATCATG
XM_011521517.2:c.127+24_127+25insATCATG	XP_011519819.1:n.127+24_127+25insATCATG
XM_017022136.1:c.1537+24_1537+25insATCATG	XP_016877625.1:n.1537+24_1537+25insATCATG
XM_017022137.1:c.1537+24_1537+25insATCATG	XP_016877626.1:n.1537+24_1537+25insATCATG
XM_017022138.1:c.1537+24_1537+25insATCATG	XP_016877627.1:n.1537+24_1537+25insATCATG
XM_017022139.1:c.1099+24_1099+25insATCATG	XP_016877628.1:n.1099+24_1099+25insATCATG
XM_024449913.1:c.553+24_553+25insATCATG	XP_024305681.1:n.553+24_553+25insATCATG
NM_000875.5:c.1462+24_1462+25insATCATG MANE Select	NP_000866.1:n.1462+24_1462+25insATCATG
NM_001291858.2:c.1462+24_1462+25insATCATG	NP_001278787.1:n.1462+24_1462+25insATCATG