Canonical Allele Identifier: CA2525105880

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146079_2146081del , CM000673.2:g.2146079_2146081del GRCh38
NC_000011.9:g.2167309_2167311del , CM000673.1:g.2167309_2167311del GRCh37
NC_000011.8:g.2123885_2123887del NCBI36
NG_008849.1:g.8526_8528del
NG_050578.1:g.20132_20134del

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1488_-7+1490del (IGF2) ENSP00000511998.1:n.-7+1488_-7+1490del
ENST00000643349.2:c.*46+1488_*46+1490del ENSP00000495715.1:n.*46+1488_*46+1490del
ENST00000695541.1:c.-7+1488_-7+1490del (IGF2) ENSP00000511997.1:n.-7+1488_-7+1490del
ENST00000643349.1:c.*46+1488_*46+1490del ENSP00000495715.1:n.*46+1488_*46+1490del
ENST00000356578.8:c.*46+1488_*46+1490del (INS-IGF2) ENSP00000348986.4:n.*46+1488_*46+1490del
NM_001007139.5:c.-7+1488_-7+1490del (IGF2) NP_001007140.2:n.-7+1488_-7+1490del
NR_003512.3:n.708+1488_708+1490del (INS-IGF2)
NR_028043.2:n.437-166_437-164del (IGF2-AS)
NR_133657.1:n.437-277_437-275del (IGF2-AS)
NR_003512.4:n.708+1488_708+1490del (INS-IGF2)
NM_001007139.6:c.-7+1488_-7+1490del (IGF2) NP_001007140.2:n.-7+1488_-7+1490del