Canonical Allele Identifier: CA934421675
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Linked Data

dbSNP Id: rs1860151729
gnomAD v3: 11-2148990-CCCT-C
gnomAD v4: 11-2148990-CCCT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2148993_2148995del , CM000673.2:g.2148993_2148995del GRCh38
NC_000011.9:g.2170223_2170225del , CM000673.1:g.2170223_2170225del GRCh37
NC_000011.8:g.2126799_2126801del NCBI36
NG_008849.1:g.5611_5613del
NG_050578.1:g.17217_17219del

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-249+133_-249+135del (IGF2) ENSP00000511998.1:n.-249+133_-249+135del
ENST00000643349.2:c.254+133_254+135del ENSP00000495715.1:n.254+133_254+135del
ENST00000695541.1:c.-249+133_-249+135del (IGF2) ENSP00000511997.1:n.-249+133_-249+135del
ENST00000481781.2:n.345+133_345+135del
ENST00000643349.1:c.254+133_254+135del ENSP00000495715.1:n.254+133_254+135del
ENST00000356578.8:c.407+133_407+135del (INS-IGF2) ENSP00000348986.4:n.407+133_407+135del
ENST00000397270.1:c.407+133_407+135del (INS-IGF2) ENSP00000380440.1:n.407+133_407+135del
ENST00000476874.1:n.423_425del (INS-IGF2)
ENST00000481781.1:n.612+133_612+135del (INS-IGF2)
NM_001007139.5:c.-249+133_-249+135del (IGF2) NP_001007140.2:n.-249+133_-249+135del
NM_001042376.2:c.407+133_407+135del (INS-IGF2) NP_001035835.1:n.407+133_407+135del
NR_003512.3:n.466+133_466+135del (INS-IGF2)
NM_001042376.3:c.407+133_407+135del (INS-IGF2) NP_001035835.1:n.407+133_407+135del
NR_003512.4:n.466+133_466+135del (INS-IGF2)
NM_001007139.6:c.-249+133_-249+135del (IGF2) NP_001007140.2:n.-249+133_-249+135del
Search 100 bp 5'
Search 100 bp 3'