Canonical Allele Identifier: CA1948015055

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146118_2146120delinsTCC , CM000673.2:g.2146118_2146120delinsTCC GRCh38
NC_000011.9:g.2167348_2167350delinsTCC , CM000673.1:g.2167348_2167350delinsTCC GRCh37
NC_000011.8:g.2123924_2123926delinsTCC NCBI36
NG_008849.1:g.8484_8486delinsGGA
NG_050578.1:g.20090_20092delinsGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1446_-7+1448delinsGGA (IGF2) ENSP00000511998.1:n.-7+1446_-7+1448delins...
ENST00000643349.2:c.*46+1446_*46+1448delinsGGA ENSP00000495715.1:n.*46+1446_*46+1448deli...
ENST00000695541.1:c.-7+1446_-7+1448delinsGGA (IGF2) ENSP00000511997.1:n.-7+1446_-7+1448delins...
ENST00000643349.1:c.*46+1446_*46+1448delinsGGA ENSP00000495715.1:n.*46+1446_*46+1448deli...
ENST00000356578.8:c.*46+1446_*46+1448delinsGGA (INS-IGF2) ENSP00000348986.4:n.*46+1446_*46+1448deli...
NM_001007139.5:c.-7+1446_-7+1448delinsGGA (IGF2) NP_001007140.2:n.-7+1446_-7+1448delinsGGA...
NR_003512.3:n.708+1446_708+1448delinsGGA (INS-IGF2)
NR_028043.2:n.437-127_437-125delinsTCC (IGF2-AS)
NR_133657.1:n.437-238_437-236delinsTCC (IGF2-AS)
NR_003512.4:n.708+1446_708+1448delinsGGA (INS-IGF2)
NM_001007139.6:c.-7+1446_-7+1448delinsGGA (IGF2) NP_001007140.2:n.-7+1446_-7+1448delinsGGA...