Canonical Allele Identifier: CA7751739
Gene: IGF1R HGNC NCBI

Linked Data

dbSNP Id: rs754690558

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98707543C>A , CM000677.2:g.98707543C>A GRCh38
NC_000015.9:g.99250772C>A , CM000677.1:g.99250772C>A GRCh37
NC_000015.8:g.97068295C>A NCBI36
NG_009492.1:g.63012C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.95-19C>A ENSP00000496919.1:n.95-19C>A
ENST00000650285.1:c.95-19C>A MANE Select ENSP00000497069.1:n.95-19C>A
ENST00000268035.10:c.95-19C>A ENSP00000268035.6:n.95-19C>A
ENST00000558762.5:c.95-19C>A ENSP00000453007.1:n.95-19C>A
ENST00000559925.5:n.95-19C>A
NM_000875.4:c.95-19C>A NP_000866.1:n.95-19C>A
NM_001291858.1:c.95-19C>A NP_001278787.1:n.95-19C>A
XM_011521513.1:c.95-19C>A XP_011519815.1:n.95-19C>A
XM_011521514.1:c.95-19C>A XP_011519816.1:n.95-19C>A
XM_011521515.1:c.95-19C>A XP_011519817.1:n.95-19C>A
XM_017022136.1:c.170-19C>A XP_016877625.1:n.170-19C>A
XM_017022137.1:c.170-19C>A XP_016877626.1:n.170-19C>A
XM_017022138.1:c.170-19C>A XP_016877627.1:n.170-19C>A
XM_017022139.1:c.-269-19C>A XP_016877628.1:n.-269-19C>A
NM_000875.5:c.95-19C>A MANE Select NP_000866.1:n.95-19C>A
NM_001291858.2:c.95-19C>A NP_001278787.1:n.95-19C>A