Canonical Allele Identifier: CA1948016429

Gene: IGF2 INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148832C= , CM000673.2:g.2148832C=	GRCh38
NC_000011.9:g.2170062C= , CM000673.1:g.2170062C=	GRCh37
NC_000011.8:g.2126638C=	NCBI36
NG_008849.1:g.5772G=
NG_050578.1:g.17378G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000481781.3:c.-249+294G= (IGF2)	ENSP00000511998.1:n.-249+294G=
ENST00000643349.2:c.254+294G=	ENSP00000495715.1:n.254+294G=
ENST00000695541.1:c.-249+294G= (IGF2)	ENSP00000511997.1:n.-249+294G=
ENST00000481781.2:n.345+294G=
ENST00000643349.1:c.254+294G=	ENSP00000495715.1:n.254+294G=
ENST00000356578.8:c.407+294G= (INS-IGF2)	ENSP00000348986.4:n.407+294G=
ENST00000397270.1:c.407+294G= (INS-IGF2)	ENSP00000380440.1:n.407+294G=
ENST00000481781.1:n.612+294G= (INS-IGF2)
NM_001007139.5:c.-249+294G= (IGF2)	NP_001007140.2:n.-249+294G=
NM_001042376.2:c.407+294G= (INS-IGF2)	NP_001035835.1:n.407+294G=
NR_003512.3:n.466+294G= (INS-IGF2)
NM_001042376.3:c.407+294G= (INS-IGF2)	NP_001035835.1:n.407+294G=
NR_003512.4:n.466+294G= (INS-IGF2)
NM_001007139.6:c.-249+294G= (IGF2)	NP_001007140.2:n.-249+294G=