Canonical Allele Identifier: CA1948014424

Linked Data

dbSNP Id: rs1859952858

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146387_2146388insGCT , CM000673.2:g.2146387_2146388insGCT GRCh38
NC_000011.9:g.2167617_2167618insGCT , CM000673.1:g.2167617_2167618insGCT GRCh37
NC_000011.8:g.2124193_2124194insGCT NCBI36
NG_008849.1:g.8216_8217insAGC
NG_050578.1:g.19822_19823insAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1178_-7+1179insAGC (IGF2) ENSP00000511998.1:n.-7+1178_-7+1179insAGC
ENST00000643349.2:c.*46+1178_*46+1179insAGC ENSP00000495715.1:n.*46+1178_*46+1179insAGC
ENST00000695541.1:c.-7+1178_-7+1179insAGC (IGF2) ENSP00000511997.1:n.-7+1178_-7+1179insAGC
ENST00000643349.1:c.*46+1178_*46+1179insAGC ENSP00000495715.1:n.*46+1178_*46+1179insAGC
ENST00000356578.8:c.*46+1178_*46+1179insAGC (INS-IGF2) ENSP00000348986.4:n.*46+1178_*46+1179insAGC
NM_001007139.5:c.-7+1178_-7+1179insAGC (IGF2) NP_001007140.2:n.-7+1178_-7+1179insAGC
NR_003512.3:n.708+1178_708+1179insAGC (INS-IGF2)
NR_028043.2:n.579_580insGCT (IGF2-AS)
NR_133657.1:n.468_469insGCT (IGF2-AS)
NR_003512.4:n.708+1178_708+1179insAGC (INS-IGF2)
NM_001007139.6:c.-7+1178_-7+1179insAGC (IGF2) NP_001007140.2:n.-7+1178_-7+1179insAGC