Canonical Allele Identifier: CA620312015

Gene: IGF1R

Linked Data

• ClinVar Variation Id: 2958794
• ClinVar RCV Id: RCV003817017
• dbSNP Id: rs1481039914
• gnomAD v2: 15-99250773-C-T
• gnomAD v3: 15-98707544-C-T
• gnomAD v4: 15-98707544-C-T
• MyVariant Identifiers: chr15:g.99250773C>T (hg19) ; chr15:g.98707544C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98707544C>T , CM000677.2:g.98707544C>T	GRCh38
NC_000015.9:g.99250773C>T , CM000677.1:g.99250773C>T	GRCh37
NC_000015.8:g.97068296C>T	NCBI36
NG_009492.1:g.63013C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.95-18C>T	ENSP00000496919.1:n.95-18C>T
ENST00000650285.1:c.95-18C>T MANE Select	ENSP00000497069.1:n.95-18C>T
ENST00000268035.10:c.95-18C>T	ENSP00000268035.6:n.95-18C>T
ENST00000558762.5:c.95-18C>T	ENSP00000453007.1:n.95-18C>T
ENST00000559925.5:n.95-18C>T
NM_000875.4:c.95-18C>T	NP_000866.1:n.95-18C>T
NM_001291858.1:c.95-18C>T	NP_001278787.1:n.95-18C>T
XM_011521513.1:c.95-18C>T	XP_011519815.1:n.95-18C>T
XM_011521514.1:c.95-18C>T	XP_011519816.1:n.95-18C>T
XM_011521515.1:c.95-18C>T	XP_011519817.1:n.95-18C>T
XM_017022136.1:c.170-18C>T	XP_016877625.1:n.170-18C>T
XM_017022137.1:c.170-18C>T	XP_016877626.1:n.170-18C>T
XM_017022138.1:c.170-18C>T	XP_016877627.1:n.170-18C>T
XM_017022139.1:c.-269-18C>T	XP_016877628.1:n.-269-18C>T
NM_000875.5:c.95-18C>T MANE Select	NP_000866.1:n.95-18C>T
NM_001291858.2:c.95-18C>T	NP_001278787.1:n.95-18C>T