Canonical Allele Identifier: CA3002974651
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2148818_2148819insG , CM000673.2:g.2148818_2148819insG GRCh38
NC_000011.9:g.2170048_2170049insG , CM000673.1:g.2170048_2170049insG GRCh37
NC_000011.8:g.2126624_2126625insG NCBI36
NG_008849.1:g.5785_5786insC
NG_050578.1:g.17391_17392insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-249+307_-249+308insC (IGF2) ENSP00000511998.1:n.-249+307_-249+308insC
ENST00000643349.2:c.254+307_254+308insC ENSP00000495715.1:n.254+307_254+308insC
ENST00000695541.1:c.-249+307_-249+308insC (IGF2) ENSP00000511997.1:n.-249+307_-249+308insC
ENST00000481781.2:n.345+307_345+308insC
ENST00000643349.1:c.254+307_254+308insC ENSP00000495715.1:n.254+307_254+308insC
ENST00000356578.8:c.407+307_407+308insC (INS-IGF2) ENSP00000348986.4:n.407+307_407+308insC
ENST00000397270.1:c.407+307_407+308insC (INS-IGF2) ENSP00000380440.1:n.407+307_407+308insC
ENST00000481781.1:n.612+307_612+308insC (INS-IGF2)
NM_001007139.5:c.-249+307_-249+308insC (IGF2) NP_001007140.2:n.-249+307_-249+308insC
NM_001042376.2:c.407+307_407+308insC (INS-IGF2) NP_001035835.1:n.407+307_407+308insC
NR_003512.3:n.466+307_466+308insC (INS-IGF2)
NM_001042376.3:c.407+307_407+308insC (INS-IGF2) NP_001035835.1:n.407+307_407+308insC
NR_003512.4:n.466+307_466+308insC (INS-IGF2)
NM_001007139.6:c.-249+307_-249+308insC (IGF2) NP_001007140.2:n.-249+307_-249+308insC