Canonical Allele Identifier: CA1948016660
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2149207C= , CM000673.2:g.2149207C= GRCh38
NC_000011.9:g.2170437C= , CM000673.1:g.2170437C= GRCh37
NC_000011.8:g.2127013C= NCBI36
NG_008849.1:g.5397G=
NG_050578.1:g.17003G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-330G= (IGF2) ENSP00000511998.1:n.-330G=
ENST00000643349.2:c.173G= ENSP00000495715.1:p.Arg58=
ENST00000695541.1:c.-330G= (IGF2) ENSP00000511997.1:n.-330G=
ENST00000481781.2:n.264G=
ENST00000643349.1:c.173G= ENSP00000495715.1:p.Arg58=
ENST00000356578.8:c.326G= (INS-IGF2) ENSP00000348986.4:p.Arg109=
ENST00000397270.1:c.326G= (INS-IGF2) ENSP00000380440.1:p.Arg109=
ENST00000476874.1:n.209G= (INS-IGF2)
ENST00000481781.1:n.531G= (INS-IGF2)
NM_001007139.5:c.-330G= (IGF2) NP_001007140.2:n.-330G=
NM_001042376.2:c.326G= (INS-IGF2) NP_001035835.1:p.Arg109=
NR_003512.3:n.385G= (INS-IGF2)
NM_001042376.3:c.326G= (INS-IGF2) NP_001035835.1:p.Arg109=
NR_003512.4:n.385G= (INS-IGF2)
NM_001007139.6:c.-330G= (IGF2) NP_001007140.2:n.-330G=