Canonical Allele Identifier: CA1948016630
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2149182_2149183delinsCG , CM000673.2:g.2149182_2149183delinsCG GRCh38
NC_000011.9:g.2170412_2170413delinsCG , CM000673.1:g.2170412_2170413delinsCG GRCh37
NC_000011.8:g.2126988_2126989delinsCG NCBI36
NG_008849.1:g.5421_5422delinsCG
NG_050578.1:g.17027_17028delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-306_-305delinsCG (IGF2) ENSP00000511998.1:n.-306_-305delinsCG
ENST00000643349.2:c.197_198delinsCG ENSP00000495715.1:p.Pro66=
ENST00000695541.1:c.-306_-305delinsCG (IGF2) ENSP00000511997.1:n.-306_-305delinsCG
ENST00000481781.2:n.288_289delinsCG
ENST00000643349.1:c.197_198delinsCG ENSP00000495715.1:p.Pro66=
ENST00000356578.8:c.350_351delinsCG (INS-IGF2) ENSP00000348986.4:p.Pro117=
ENST00000397270.1:c.350_351delinsCG (INS-IGF2) ENSP00000380440.1:p.Pro117=
ENST00000476874.1:n.233_234delinsCG (INS-IGF2)
ENST00000481781.1:n.555_556delinsCG (INS-IGF2)
NM_001007139.5:c.-306_-305delinsCG (IGF2) NP_001007140.2:n.-306_-305delinsCG
NM_001042376.2:c.350_351delinsCG (INS-IGF2) NP_001035835.1:p.Pro117=
NR_003512.3:n.409_410delinsCG (INS-IGF2)
NM_001042376.3:c.350_351delinsCG (INS-IGF2) NP_001035835.1:p.Pro117=
NR_003512.4:n.409_410delinsCG (INS-IGF2)
NM_001007139.6:c.-306_-305delinsCG (IGF2) NP_001007140.2:n.-306_-305delinsCG