Canonical Allele Identifier: CA1948015035

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146093_2146094delinsAC , CM000673.2:g.2146093_2146094delinsAC GRCh38
NC_000011.9:g.2167323_2167324delinsAC , CM000673.1:g.2167323_2167324delinsAC GRCh37
NC_000011.8:g.2123899_2123900delinsAC NCBI36
NG_008849.1:g.8510_8511delinsGT
NG_050578.1:g.20116_20117delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1472_-7+1473delinsGT (IGF2) ENSP00000511998.1:n.-7+1472_-7+1473delinsGT
ENST00000643349.2:c.*46+1472_*46+1473delinsGT ENSP00000495715.1:n.*46+1472_*46+1473delinsGT
ENST00000695541.1:c.-7+1472_-7+1473delinsGT (IGF2) ENSP00000511997.1:n.-7+1472_-7+1473delinsGT
ENST00000643349.1:c.*46+1472_*46+1473delinsGT ENSP00000495715.1:n.*46+1472_*46+1473delinsGT
ENST00000356578.8:c.*46+1472_*46+1473delinsGT (INS-IGF2) ENSP00000348986.4:n.*46+1472_*46+1473delinsGT
NM_001007139.5:c.-7+1472_-7+1473delinsGT (IGF2) NP_001007140.2:n.-7+1472_-7+1473delinsGT
NR_003512.3:n.708+1472_708+1473delinsGT (INS-IGF2)
NR_028043.2:n.437-152_437-151delinsAC (IGF2-AS)
NR_133657.1:n.437-263_437-262delinsAC (IGF2-AS)
NR_003512.4:n.708+1472_708+1473delinsGT (INS-IGF2)
NM_001007139.6:c.-7+1472_-7+1473delinsGT (IGF2) NP_001007140.2:n.-7+1472_-7+1473delinsGT