Canonical Allele Identifier: CA1948015103

Linked Data

dbSNP Id: rs1859922957

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146147_2146160del , CM000673.2:g.2146147_2146160del GRCh38
NC_000011.9:g.2167377_2167390del , CM000673.1:g.2167377_2167390del GRCh37
NC_000011.8:g.2123953_2123966del NCBI36
NG_008849.1:g.8450_8463del
NG_050578.1:g.20056_20069del

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1412_-7+1425del (IGF2) ENSP00000511998.1:n.-7+1412_-7+1425del
ENST00000643349.2:c.*46+1412_*46+1425del ENSP00000495715.1:n.*46+1412_*46+1425del
ENST00000695541.1:c.-7+1412_-7+1425del (IGF2) ENSP00000511997.1:n.-7+1412_-7+1425del
ENST00000643349.1:c.*46+1412_*46+1425del ENSP00000495715.1:n.*46+1412_*46+1425del
ENST00000356578.8:c.*46+1412_*46+1425del (INS-IGF2) ENSP00000348986.4:n.*46+1412_*46+1425del
NM_001007139.5:c.-7+1412_-7+1425del (IGF2) NP_001007140.2:n.-7+1412_-7+1425del
NR_003512.3:n.708+1412_708+1425del (INS-IGF2)
NR_028043.2:n.437-98_437-85del (IGF2-AS)
NR_133657.1:n.437-209_437-196del (IGF2-AS)
NR_003512.4:n.708+1412_708+1425del (INS-IGF2)
NM_001007139.6:c.-7+1412_-7+1425del (IGF2) NP_001007140.2:n.-7+1412_-7+1425del