Canonical Allele Identifier: CA275326614

Gene: IGF1R

Linked Data

• dbSNP Id: rs933214456
• gnomAD v2: 15-99478456-C-T
• gnomAD v3: 15-98935227-C-T
• gnomAD v4: 15-98935227-C-T
• MyVariant Identifiers: chr15:g.99478456C>T (hg19) ; chr15:g.98935227C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98935227C>T , CM000677.2:g.98935227C>T	GRCh38
NC_000015.9:g.99478456C>T , CM000677.1:g.99478456C>T	GRCh37
NC_000015.8:g.97295979C>T	NCBI36
NG_009492.1:g.290696C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.3184-89C>T	ENSP00000496919.1:n.3184-89C>T
ENST00000650285.1:c.3187-89C>T MANE Select	ENSP00000497069.1:n.3187-89C>T
ENST00000268035.10:c.3187-89C>T	ENSP00000268035.6:n.3187-89C>T
ENST00000558762.5:c.3184-89C>T	ENSP00000453007.1:n.3184-89C>T
ENST00000560972.1:c.260-89C>T	ENSP00000453180.1:n.260-89C>T
NM_000875.4:c.3187-89C>T	NP_000866.1:n.3187-89C>T
NM_001291858.1:c.3184-89C>T	NP_001278787.1:n.3184-89C>T
XM_011521513.1:c.3250-89C>T	XP_011519815.1:n.3250-89C>T
XM_011521514.1:c.3250-89C>T	XP_011519816.1:n.3250-89C>T
XM_011521515.1:c.3247-89C>T	XP_011519817.1:n.3247-89C>T
XM_011521516.1:c.2278-89C>T	XP_011519818.1:n.2278-89C>T
XM_011521517.1:c.1852-89C>T	XP_011519819.1:n.1852-89C>T
XM_011521516.2:c.2278-89C>T	XP_011519818.1:n.2278-89C>T
XM_011521517.2:c.1852-89C>T	XP_011519819.1:n.1852-89C>T
XM_017022136.1:c.3262-89C>T	XP_016877625.1:n.3262-89C>T
XM_017022137.1:c.3262-89C>T	XP_016877626.1:n.3262-89C>T
XM_017022138.1:c.3259-89C>T	XP_016877627.1:n.3259-89C>T
XM_017022139.1:c.2824-89C>T	XP_016877628.1:n.2824-89C>T
XM_024449913.1:c.2278-89C>T	XP_024305681.1:n.2278-89C>T
NM_000875.5:c.3187-89C>T MANE Select	NP_000866.1:n.3187-89C>T
NM_001291858.2:c.3184-89C>T	NP_001278787.1:n.3184-89C>T