Canonical Allele Identifier: CA2611958417

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146403_2146407dup , CM000673.2:g.2146403_2146407dup GRCh38
NC_000011.9:g.2167633_2167637dup , CM000673.1:g.2167633_2167637dup GRCh37
NC_000011.8:g.2124209_2124213dup NCBI36
NG_008849.1:g.8199_8203dup
NG_050578.1:g.19805_19809dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1161_-7+1165dup (IGF2) ENSP00000511998.1:n.-7+1161_-7+1165dup
ENST00000643349.2:c.*46+1161_*46+1165dup ENSP00000495715.1:n.*46+1161_*46+1165dup
ENST00000695541.1:c.-7+1161_-7+1165dup (IGF2) ENSP00000511997.1:n.-7+1161_-7+1165dup
ENST00000643349.1:c.*46+1161_*46+1165dup ENSP00000495715.1:n.*46+1161_*46+1165dup
ENST00000356578.8:c.*46+1161_*46+1165dup (INS-IGF2) ENSP00000348986.4:n.*46+1161_*46+1165dup
NM_001007139.5:c.-7+1161_-7+1165dup (IGF2) NP_001007140.2:n.-7+1161_-7+1165dup
NR_003512.3:n.708+1161_708+1165dup (INS-IGF2)
NR_028043.2:n.595_599dup (IGF2-AS)
NR_133657.1:n.484_488dup (IGF2-AS)
NR_003512.4:n.708+1161_708+1165dup (INS-IGF2)
NM_001007139.6:c.-7+1161_-7+1165dup (IGF2) NP_001007140.2:n.-7+1161_-7+1165dup