Canonical Allele Identifier: CA2611956981

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146109_2146111del , CM000673.2:g.2146109_2146111del GRCh38
NC_000011.9:g.2167339_2167341del , CM000673.1:g.2167339_2167341del GRCh37
NC_000011.8:g.2123915_2123917del NCBI36
NG_008849.1:g.8495_8497del
NG_050578.1:g.20101_20103del

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1457_-7+1459del (IGF2) ENSP00000511998.1:n.-7+1457_-7+1459del
ENST00000643349.2:c.*46+1457_*46+1459del ENSP00000495715.1:n.*46+1457_*46+1459del
ENST00000695541.1:c.-7+1457_-7+1459del (IGF2) ENSP00000511997.1:n.-7+1457_-7+1459del
ENST00000643349.1:c.*46+1457_*46+1459del ENSP00000495715.1:n.*46+1457_*46+1459del
ENST00000356578.8:c.*46+1457_*46+1459del (INS-IGF2) ENSP00000348986.4:n.*46+1457_*46+1459del
NM_001007139.5:c.-7+1457_-7+1459del (IGF2) NP_001007140.2:n.-7+1457_-7+1459del
NR_003512.3:n.708+1457_708+1459del (INS-IGF2)
NR_028043.2:n.437-136_437-134del (IGF2-AS)
NR_133657.1:n.437-247_437-245del (IGF2-AS)
NR_003512.4:n.708+1457_708+1459del (INS-IGF2)
NM_001007139.6:c.-7+1457_-7+1459del (IGF2) NP_001007140.2:n.-7+1457_-7+1459del