Canonical Allele Identifier: CA1948015601

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146366_2146384delinsACGAGGCGCTGACCTTGCG , CM000673.2:g.2146366_2146384delinsACGAGGCGCTGACCTTGCG GRCh38
NC_000011.9:g.2167596_2167614delinsACGAGGCGCTGACCTTGCG , CM000673.1:g.2167596_2167614delinsACGAGGCGCTGACCTTGCG GRCh37
NC_000011.8:g.2124172_2124190delinsACGAGGCGCTGACCTTGCG NCBI36
NG_008849.1:g.8220_8238delinsCGCAAGGTCAGCGCCTCGT
NG_050578.1:g.19826_19844delinsCGCAAGGTCAGCGCCTCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1182_-7+1200delinsCGCAAGGTCAGCGCCTCGT (IGF2) ENSP00000511998.1:n.-7+1182_-7+1200delinsCGCAAGGTCAGCGCCTCGT
ENST00000643349.2:c.*46+1182_*46+1200delinsCGCAAGGTCAGCGCCTCGT ENSP00000495715.1:n.*46+1182_*46+1200delinsCGCAAGGTCAGCGCCTCG...
ENST00000695541.1:c.-7+1182_-7+1200delinsCGCAAGGTCAGCGCCTCGT (IGF2) ENSP00000511997.1:n.-7+1182_-7+1200delinsCGCAAGGTCAGCGCCTCGT
ENST00000643349.1:c.*46+1182_*46+1200delinsCGCAAGGTCAGCGCCTCGT ENSP00000495715.1:n.*46+1182_*46+1200delinsCGCAAGGTCAGCGCCTCG...
ENST00000356578.8:c.*46+1182_*46+1200delinsCGCAAGGTCAGCGCCTCGT (INS-IGF2) ENSP00000348986.4:n.*46+1182_*46+1200delinsCGCAAGGTCAGCGCCTCG...
NM_001007139.5:c.-7+1182_-7+1200delinsCGCAAGGTCAGCGCCTCGT (IGF2) NP_001007140.2:n.-7+1182_-7+1200delinsCGCAAGGTCAGCGCCTCGT
NR_003512.3:n.708+1182_708+1200delinsCGCAAGGTCAGCGCCTCGT (INS-IGF2)
NR_028043.2:n.558_576delinsACGAGGCGCTGACCTTGCG (IGF2-AS)
NR_133657.1:n.447_465delinsACGAGGCGCTGACCTTGCG (IGF2-AS)
NR_003512.4:n.708+1182_708+1200delinsCGCAAGGTCAGCGCCTCGT (INS-IGF2)
NM_001007139.6:c.-7+1182_-7+1200delinsCGCAAGGTCAGCGCCTCGT (IGF2) NP_001007140.2:n.-7+1182_-7+1200delinsCGCAAGGTCAGCGCCTCGT