Canonical Allele Identifier: CA216260207

Linked Data

dbSNP Id: rs17882671

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146122dup , CM000673.2:g.2146122dup GRCh38
NC_000011.9:g.2167352dup , CM000673.1:g.2167352dup GRCh37
NC_000011.8:g.2123928dup NCBI36
NG_008849.1:g.8485dup
NG_050578.1:g.20091dup

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1447dup (IGF2) ENSP00000511998.1:n.-7+1447dup
ENST00000643349.2:c.*46+1447dup ENSP00000495715.1:n.*46+1447dup
ENST00000695541.1:c.-7+1447dup (IGF2) ENSP00000511997.1:n.-7+1447dup
ENST00000643349.1:c.*46+1447dup ENSP00000495715.1:n.*46+1447dup
ENST00000356578.8:c.*46+1447dup (INS-IGF2) ENSP00000348986.4:n.*46+1447dup
NM_001007139.5:c.-7+1447dup (IGF2) NP_001007140.2:n.-7+1447dup
NR_003512.3:n.708+1447dup (INS-IGF2)
NR_028043.2:n.437-123dup (IGF2-AS)
NR_133657.1:n.437-234dup (IGF2-AS)
NR_003512.4:n.708+1447dup (INS-IGF2)
NM_001007139.6:c.-7+1447dup (IGF2) NP_001007140.2:n.-7+1447dup