Canonical Allele Identifier: CA1948016726
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2149272_2149273delinsAG , CM000673.2:g.2149272_2149273delinsAG GRCh38
NC_000011.9:g.2170502_2170503delinsAG , CM000673.1:g.2170502_2170503delinsAG GRCh37
NC_000011.8:g.2127078_2127079delinsAG NCBI36
NG_008849.1:g.5331_5332delinsCT
NG_050578.1:g.16937_16938delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-396_-395delinsCT (IGF2) ENSP00000511998.1:n.-396_-395delinsCT
ENST00000643349.2:c.107_108delinsCT ENSP00000495715.1:p.Pro36=
ENST00000695541.1:c.-396_-395delinsCT (IGF2) ENSP00000511997.1:n.-396_-395delinsCT
ENST00000481781.2:n.198_199delinsCT
ENST00000643349.1:c.107_108delinsCT ENSP00000495715.1:p.Pro36=
ENST00000356578.8:c.260_261delinsCT (INS-IGF2) ENSP00000348986.4:p.Pro87=
ENST00000397270.1:c.260_261delinsCT (INS-IGF2) ENSP00000380440.1:p.Pro87=
ENST00000476874.1:n.143_144delinsCT (INS-IGF2)
ENST00000481781.1:n.465_466delinsCT (INS-IGF2)
NM_001007139.5:c.-396_-395delinsCT (IGF2) NP_001007140.2:n.-396_-395delinsCT
NM_001042376.2:c.260_261delinsCT (INS-IGF2) NP_001035835.1:p.Pro87=
NR_003512.3:n.319_320delinsCT (INS-IGF2)
NM_001042376.3:c.260_261delinsCT (INS-IGF2) NP_001035835.1:p.Pro87=
NR_003512.4:n.319_320delinsCT (INS-IGF2)
NM_001007139.6:c.-396_-395delinsCT (IGF2) NP_001007140.2:n.-396_-395delinsCT