Canonical Allele Identifier: CA1948016831
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2149386A= , CM000673.2:g.2149386A= GRCh38
NC_000011.9:g.2170616A= , CM000673.1:g.2170616A= GRCh37
NC_000011.8:g.2127192A= NCBI36
NG_008849.1:g.5218T=
NG_050578.1:g.16824T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-468-41T= (IGF2) ENSP00000511998.1:n.-468-41T=
ENST00000643349.2:c.-7T= ENSP00000495715.1:n.-7T=
ENST00000695541.1:c.-468-41T= (IGF2) ENSP00000511997.1:n.-468-41T=
ENST00000481781.2:n.126-41T=
ENST00000643349.1:c.-7T= ENSP00000495715.1:n.-7T=
ENST00000356578.8:c.188-41T= (INS-IGF2) ENSP00000348986.4:n.188-41T=
ENST00000397270.1:c.188-41T= (INS-IGF2) ENSP00000380440.1:n.188-41T=
ENST00000476874.1:n.71-41T= (INS-IGF2)
ENST00000481781.1:n.393-41T= (INS-IGF2)
NM_001007139.5:c.-509T= (IGF2) NP_001007140.2:n.-509T=
NM_001042376.2:c.188-41T= (INS-IGF2) NP_001035835.1:n.188-41T=
NR_003512.3:n.247-41T= (INS-IGF2)
NM_001042376.3:c.188-41T= (INS-IGF2) NP_001035835.1:n.188-41T=
NR_003512.4:n.247-41T= (INS-IGF2)
NM_001007139.6:c.-509T= (IGF2) NP_001007140.2:n.-509T=