Canonical Allele Identifier: CA1948015587

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146364_2146375delinsAGACGAGGCGCT , CM000673.2:g.2146364_2146375delinsAGACGAGGCGCT GRCh38
NC_000011.9:g.2167594_2167605delinsAGACGAGGCGCT , CM000673.1:g.2167594_2167605delinsAGACGAGGCGCT GRCh37
NC_000011.8:g.2124170_2124181delinsAGACGAGGCGCT NCBI36
NG_008849.1:g.8229_8240delinsAGCGCCTCGTCT
NG_050578.1:g.19835_19846delinsAGCGCCTCGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1191_-7+1202delinsAGCGCCTCGTCT (IGF2) ENSP00000511998.1:n.-7+1191_-7+1202delinsAGCGCCTCGTCT
ENST00000643349.2:c.*46+1191_*46+1202delinsAGCGCCTCGTCT ENSP00000495715.1:n.*46+1191_*46+1202delinsAGCGCCTCGTCT
ENST00000695541.1:c.-7+1191_-7+1202delinsAGCGCCTCGTCT (IGF2) ENSP00000511997.1:n.-7+1191_-7+1202delinsAGCGCCTCGTCT
ENST00000643349.1:c.*46+1191_*46+1202delinsAGCGCCTCGTCT ENSP00000495715.1:n.*46+1191_*46+1202delinsAGCGCCTCGTCT
ENST00000356578.8:c.*46+1191_*46+1202delinsAGCGCCTCGTCT (INS-IGF2) ENSP00000348986.4:n.*46+1191_*46+1202delinsAGCGCCTCGTCT
NM_001007139.5:c.-7+1191_-7+1202delinsAGCGCCTCGTCT (IGF2) NP_001007140.2:n.-7+1191_-7+1202delinsAGCGCCTCGTCT
NR_003512.3:n.708+1191_708+1202delinsAGCGCCTCGTCT (INS-IGF2)
NR_028043.2:n.556_567delinsAGACGAGGCGCT (IGF2-AS)
NR_133657.1:n.445_456delinsAGACGAGGCGCT (IGF2-AS)
NR_003512.4:n.708+1191_708+1202delinsAGCGCCTCGTCT (INS-IGF2)
NM_001007139.6:c.-7+1191_-7+1202delinsAGCGCCTCGTCT (IGF2) NP_001007140.2:n.-7+1191_-7+1202delinsAGCGCCTCGTCT