Canonical Allele Identifier: CA2199176997
Gene: IGF1R HGNC NCBI

Linked Data

dbSNP Id: rs2053894494

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98707529_98707532del , CM000677.2:g.98707529_98707532del GRCh38
NC_000015.9:g.99250758_99250761del , CM000677.1:g.99250758_99250761del GRCh37
NC_000015.8:g.97068281_97068284del NCBI36
NG_009492.1:g.62998_63001del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649865.1:c.95-33_95-30del ENSP00000496919.1:n.95-33_95-30del
ENST00000650285.1:c.95-33_95-30del MANE Select ENSP00000497069.1:n.95-33_95-30del
ENST00000268035.10:c.95-33_95-30del ENSP00000268035.6:n.95-33_95-30del
ENST00000558762.5:c.95-33_95-30del ENSP00000453007.1:n.95-33_95-30del
ENST00000559925.5:n.95-33_95-30del
NM_000875.4:c.95-33_95-30del NP_000866.1:n.95-33_95-30del
NM_001291858.1:c.95-33_95-30del NP_001278787.1:n.95-33_95-30del
XM_011521513.1:c.95-33_95-30del XP_011519815.1:n.95-33_95-30del
XM_011521514.1:c.95-33_95-30del XP_011519816.1:n.95-33_95-30del
XM_011521515.1:c.95-33_95-30del XP_011519817.1:n.95-33_95-30del
XM_017022136.1:c.170-33_170-30del XP_016877625.1:n.170-33_170-30del
XM_017022137.1:c.170-33_170-30del XP_016877626.1:n.170-33_170-30del
XM_017022138.1:c.170-33_170-30del XP_016877627.1:n.170-33_170-30del
XM_017022139.1:c.-269-33_-269-30del XP_016877628.1:n.-269-33_-269-30del
NM_000875.5:c.95-33_95-30del MANE Select NP_000866.1:n.95-33_95-30del
NM_001291858.2:c.95-33_95-30del NP_001278787.1:n.95-33_95-30del