Canonical Allele Identifier: CA216262132
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Linked Data

dbSNP Id: rs763072070

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2148885_2148887del , CM000673.2:g.2148885_2148887del GRCh38
NC_000011.9:g.2170115_2170117del , CM000673.1:g.2170115_2170117del GRCh37
NC_000011.8:g.2126691_2126693del NCBI36
NG_008849.1:g.5717_5719del
NG_050578.1:g.17323_17325del

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-249+239_-249+241del (IGF2) ENSP00000511998.1:n.-249+239_-249+241del
ENST00000643349.2:c.254+239_254+241del ENSP00000495715.1:n.254+239_254+241del
ENST00000695541.1:c.-249+239_-249+241del (IGF2) ENSP00000511997.1:n.-249+239_-249+241del
ENST00000481781.2:n.345+239_345+241del
ENST00000643349.1:c.254+239_254+241del ENSP00000495715.1:n.254+239_254+241del
ENST00000356578.8:c.407+239_407+241del (INS-IGF2) ENSP00000348986.4:n.407+239_407+241del
ENST00000397270.1:c.407+239_407+241del (INS-IGF2) ENSP00000380440.1:n.407+239_407+241del
ENST00000481781.1:n.612+239_612+241del (INS-IGF2)
NM_001007139.5:c.-249+239_-249+241del (IGF2) NP_001007140.2:n.-249+239_-249+241del
NM_001042376.2:c.407+239_407+241del (INS-IGF2) NP_001035835.1:n.407+239_407+241del
NR_003512.3:n.466+239_466+241del (INS-IGF2)
NM_001042376.3:c.407+239_407+241del (INS-IGF2) NP_001035835.1:n.407+239_407+241del
NR_003512.4:n.466+239_466+241del (INS-IGF2)
NM_001007139.6:c.-249+239_-249+241del (IGF2) NP_001007140.2:n.-249+239_-249+241del