Canonical Allele Identifier: CA934420938

Linked Data

dbSNP Id: rs1859926126

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146172_2146176dup , CM000673.2:g.2146172_2146176dup GRCh38
NC_000011.9:g.2167402_2167406dup , CM000673.1:g.2167402_2167406dup GRCh37
NC_000011.8:g.2123978_2123982dup NCBI36
NG_008849.1:g.8429_8433dup
NG_050578.1:g.20035_20039dup

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1391_-7+1395dup (IGF2) ENSP00000511998.1:n.-7+1391_-7+1395dup
ENST00000643349.2:c.*46+1391_*46+1395dup ENSP00000495715.1:n.*46+1391_*46+1395dup
ENST00000695541.1:c.-7+1391_-7+1395dup (IGF2) ENSP00000511997.1:n.-7+1391_-7+1395dup
ENST00000643349.1:c.*46+1391_*46+1395dup ENSP00000495715.1:n.*46+1391_*46+1395dup
ENST00000356578.8:c.*46+1391_*46+1395dup (INS-IGF2) ENSP00000348986.4:n.*46+1391_*46+1395dup
NM_001007139.5:c.-7+1391_-7+1395dup (IGF2) NP_001007140.2:n.-7+1391_-7+1395dup
NR_003512.3:n.708+1391_708+1395dup (INS-IGF2)
NR_028043.2:n.437-73_437-69dup (IGF2-AS)
NR_133657.1:n.437-184_437-180dup (IGF2-AS)
NR_003512.4:n.708+1391_708+1395dup (INS-IGF2)
NM_001007139.6:c.-7+1391_-7+1395dup (IGF2) NP_001007140.2:n.-7+1391_-7+1395dup