Canonical Allele Identifier: CA1948015099

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146140_2146154delinsCCCCATGGAGCCTGG , CM000673.2:g.2146140_2146154delinsCCCCATGGAGCCTGG GRCh38
NC_000011.9:g.2167370_2167384delinsCCCCATGGAGCCTGG , CM000673.1:g.2167370_2167384delinsCCCCATGGAGCCTGG GRCh37
NC_000011.8:g.2123946_2123960delinsCCCCATGGAGCCTGG NCBI36
NG_008849.1:g.8450_8464delinsCCAGGCTCCATGGGG
NG_050578.1:g.20056_20070delinsCCAGGCTCCATGGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1412_-7+1426delinsCCAGGCTCCATGGGG (IGF2) ENSP00000511998.1:n.-7+1412_-7+1426delins...
ENST00000643349.2:c.*46+1412_*46+1426delinsCCAGGCTCCATGGGG ENSP00000495715.1:n.*46+1412_*46+1426deli...
ENST00000695541.1:c.-7+1412_-7+1426delinsCCAGGCTCCATGGGG (IGF2) ENSP00000511997.1:n.-7+1412_-7+1426delins...
ENST00000643349.1:c.*46+1412_*46+1426delinsCCAGGCTCCATGGGG ENSP00000495715.1:n.*46+1412_*46+1426deli...
ENST00000356578.8:c.*46+1412_*46+1426delinsCCAGGCTCCATGGGG (INS-IGF2) ENSP00000348986.4:n.*46+1412_*46+1426deli...
NM_001007139.5:c.-7+1412_-7+1426delinsCCAGGCTCCATGGGG (IGF2) NP_001007140.2:n.-7+1412_-7+1426delinsCCA...
NR_003512.3:n.708+1412_708+1426delinsCCAGGCTCCATGGGG (INS-IGF2)
NR_028043.2:n.437-105_437-91delinsCCCCATGGAGCCTGG (IGF2-AS)
NR_133657.1:n.437-216_437-202delinsCCCCATGGAGCCTGG (IGF2-AS)
NR_003512.4:n.708+1412_708+1426delinsCCAGGCTCCATGGGG (INS-IGF2)
NM_001007139.6:c.-7+1412_-7+1426delinsCCAGGCTCCATGGGG (IGF2) NP_001007140.2:n.-7+1412_-7+1426delinsCCA...