Canonical Allele Identifier: CA1948014493

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146407G= , CM000673.2:g.2146407G= GRCh38
NC_000011.9:g.2167637G= , CM000673.1:g.2167637G= GRCh37
NC_000011.8:g.2124213G= NCBI36
NG_008849.1:g.8197C=
NG_050578.1:g.19803C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1159C= (IGF2) ENSP00000511998.1:n.-7+1159C=
ENST00000643349.2:c.*46+1159C= ENSP00000495715.1:n.*46+1159C=
ENST00000695541.1:c.-7+1159C= (IGF2) ENSP00000511997.1:n.-7+1159C=
ENST00000643349.1:c.*46+1159C= ENSP00000495715.1:n.*46+1159C=
ENST00000356578.8:c.*46+1159C= (INS-IGF2) ENSP00000348986.4:n.*46+1159C=
NM_001007139.5:c.-7+1159C= (IGF2) NP_001007140.2:n.-7+1159C=
NR_003512.3:n.708+1159C= (INS-IGF2)
NR_028043.2:n.599G= (IGF2-AS)
NR_133657.1:n.488G= (IGF2-AS)
NR_003512.4:n.708+1159C= (INS-IGF2)
NM_001007139.6:c.-7+1159C= (IGF2) NP_001007140.2:n.-7+1159C=