Canonical Allele Identifier: CA1948016782
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Linked Data

dbSNP Id: rs1860176169

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2149328del , CM000673.2:g.2149328del GRCh38
NC_000011.9:g.2170558del , CM000673.1:g.2170558del GRCh37
NC_000011.8:g.2127134del NCBI36
NG_008849.1:g.5276del
NG_050578.1:g.16882del

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-451del (IGF2) ENSP00000511998.1:n.-451del
ENST00000643349.2:c.52del ENSP00000495715.1:p.Ser18ProfsTer23
ENST00000695541.1:c.-451del (IGF2) ENSP00000511997.1:n.-451del
ENST00000481781.2:n.143del
ENST00000643349.1:c.52del ENSP00000495715.1:p.Ser18ProfsTer23
ENST00000356578.8:c.205del (INS-IGF2) ENSP00000348986.4:p.Ser69ProfsTer23
ENST00000397270.1:c.205del (INS-IGF2) ENSP00000380440.1:p.Ser69ProfsTer23
ENST00000476874.1:n.88del (INS-IGF2)
ENST00000481781.1:n.410del (INS-IGF2)
NM_001007139.5:c.-451del (IGF2) NP_001007140.2:n.-451del
NM_001042376.2:c.205del (INS-IGF2) NP_001035835.1:p.Ser69ProfsTer23
NR_003512.3:n.264del (INS-IGF2)
NM_001042376.3:c.205del (INS-IGF2) NP_001035835.1:p.Ser69ProfsTer23
NR_003512.4:n.264del (INS-IGF2)
NM_001007139.6:c.-451del (IGF2) NP_001007140.2:n.-451del