Canonical Allele Identifier: CA1948015069

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146122_2146123delinsCT , CM000673.2:g.2146122_2146123delinsCT GRCh38
NC_000011.9:g.2167352_2167353delinsCT , CM000673.1:g.2167352_2167353delinsCT GRCh37
NC_000011.8:g.2123928_2123929delinsCT NCBI36
NG_008849.1:g.8481_8482delinsAG
NG_050578.1:g.20087_20088delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1443_-7+1444delinsAG (IGF2) ENSP00000511998.1:n.-7+1443_-7+1444delins...
ENST00000643349.2:c.*46+1443_*46+1444delinsAG ENSP00000495715.1:n.*46+1443_*46+1444deli...
ENST00000695541.1:c.-7+1443_-7+1444delinsAG (IGF2) ENSP00000511997.1:n.-7+1443_-7+1444delins...
ENST00000643349.1:c.*46+1443_*46+1444delinsAG ENSP00000495715.1:n.*46+1443_*46+1444deli...
ENST00000356578.8:c.*46+1443_*46+1444delinsAG (INS-IGF2) ENSP00000348986.4:n.*46+1443_*46+1444deli...
NM_001007139.5:c.-7+1443_-7+1444delinsAG (IGF2) NP_001007140.2:n.-7+1443_-7+1444delinsAG
NR_003512.3:n.708+1443_708+1444delinsAG (INS-IGF2)
NR_028043.2:n.437-123_437-122delinsCT (IGF2-AS)
NR_133657.1:n.437-234_437-233delinsCT (IGF2-AS)
NR_003512.4:n.708+1443_708+1444delinsAG (INS-IGF2)
NM_001007139.6:c.-7+1443_-7+1444delinsAG (IGF2) NP_001007140.2:n.-7+1443_-7+1444delinsAG