Canonical Allele Identifier: CA674543999

Linked Data

dbSNP Id: rs1554917548

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146274_2146277dup , CM000673.2:g.2146274_2146277dup GRCh38
NC_000011.9:g.2167504_2167507dup , CM000673.1:g.2167504_2167507dup GRCh37
NC_000011.8:g.2124080_2124083dup NCBI36
NG_008849.1:g.8331_8334dup
NG_050578.1:g.19937_19940dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1293_-7+1296dup (IGF2) ENSP00000511998.1:n.-7+1293_-7+1296dup
ENST00000643349.2:c.*46+1293_*46+1296dup ENSP00000495715.1:n.*46+1293_*46+1296dup
ENST00000695541.1:c.-7+1293_-7+1296dup (IGF2) ENSP00000511997.1:n.-7+1293_-7+1296dup
ENST00000643349.1:c.*46+1293_*46+1296dup ENSP00000495715.1:n.*46+1293_*46+1296dup
ENST00000356578.8:c.*46+1293_*46+1296dup (INS-IGF2) ENSP00000348986.4:n.*46+1293_*46+1296dup
NM_001007139.5:c.-7+1293_-7+1296dup (IGF2) NP_001007140.2:n.-7+1293_-7+1296dup
NR_003512.3:n.708+1293_708+1296dup (INS-IGF2)
NR_028043.2:n.466_469dup (IGF2-AS)
NR_133657.1:n.437-82_437-79dup (IGF2-AS)
NR_003512.4:n.708+1293_708+1296dup (INS-IGF2)
NM_001007139.6:c.-7+1293_-7+1296dup (IGF2) NP_001007140.2:n.-7+1293_-7+1296dup