Canonical Allele Identifier: CA597431581

Linked Data

dbSNP Id: rs1464155217

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146364_2146374del , CM000673.2:g.2146364_2146374del GRCh38
NC_000011.9:g.2167594_2167604del , CM000673.1:g.2167594_2167604del GRCh37
NC_000011.8:g.2124170_2124180del NCBI36
NG_008849.1:g.8233_8243del
NG_050578.1:g.19839_19849del

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1195_-7+1205del (IGF2) ENSP00000511998.1:n.-7+1195_-7+1205del
ENST00000643349.2:c.*46+1195_*46+1205del ENSP00000495715.1:n.*46+1195_*46+1205del
ENST00000695541.1:c.-7+1195_-7+1205del (IGF2) ENSP00000511997.1:n.-7+1195_-7+1205del
ENST00000643349.1:c.*46+1195_*46+1205del ENSP00000495715.1:n.*46+1195_*46+1205del
ENST00000356578.8:c.*46+1195_*46+1205del (INS-IGF2) ENSP00000348986.4:n.*46+1195_*46+1205del
NM_001007139.5:c.-7+1195_-7+1205del (IGF2) NP_001007140.2:n.-7+1195_-7+1205del
NR_003512.3:n.708+1195_708+1205del (INS-IGF2)
NR_028043.2:n.556_566del (IGF2-AS)
NR_133657.1:n.445_455del (IGF2-AS)
NR_003512.4:n.708+1195_708+1205del (INS-IGF2)
NM_001007139.6:c.-7+1195_-7+1205del (IGF2) NP_001007140.2:n.-7+1195_-7+1205del