Canonical Allele Identifier: CA5817899

Linked Data

dbSNP Id: rs751221447

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146270_2146276dup , CM000673.2:g.2146270_2146276dup GRCh38
NC_000011.9:g.2167500_2167506dup , CM000673.1:g.2167500_2167506dup GRCh37
NC_000011.8:g.2124076_2124082dup NCBI36
NG_008849.1:g.8332_8338dup
NG_050578.1:g.19938_19944dup

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1294_-7+1300dup (IGF2) ENSP00000511998.1:n.-7+1294_-7+1300dup
ENST00000643349.2:c.*46+1294_*46+1300dup ENSP00000495715.1:n.*46+1294_*46+1300dup
ENST00000695541.1:c.-7+1294_-7+1300dup (IGF2) ENSP00000511997.1:n.-7+1294_-7+1300dup
ENST00000643349.1:c.*46+1294_*46+1300dup ENSP00000495715.1:n.*46+1294_*46+1300dup
ENST00000356578.8:c.*46+1294_*46+1300dup (INS-IGF2) ENSP00000348986.4:n.*46+1294_*46+1300dup
NM_001007139.5:c.-7+1294_-7+1300dup (IGF2) NP_001007140.2:n.-7+1294_-7+1300dup
NR_003512.3:n.708+1294_708+1300dup (INS-IGF2)
NR_028043.2:n.462_468dup (IGF2-AS)
NR_133657.1:n.437-86_437-80dup (IGF2-AS)
NR_003512.4:n.708+1294_708+1300dup (INS-IGF2)
NM_001007139.6:c.-7+1294_-7+1300dup (IGF2) NP_001007140.2:n.-7+1294_-7+1300dup