Canonical Allele Identifier: CA1948016699

Gene: IGF2 INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149239G= , CM000673.2:g.2149239G=	GRCh38
NC_000011.9:g.2170469G= , CM000673.1:g.2170469G=	GRCh37
NC_000011.8:g.2127045G=	NCBI36
NG_008849.1:g.5365C=
NG_050578.1:g.16971C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-362C= (IGF2)	ENSP00000511998.1:n.-362C=
ENST00000643349.2:c.141C=	ENSP00000495715.1:p.Ala47=
ENST00000695541.1:c.-362C= (IGF2)	ENSP00000511997.1:n.-362C=
ENST00000481781.2:n.232C=
ENST00000643349.1:c.141C=	ENSP00000495715.1:p.Ala47=
ENST00000356578.8:c.294C= (INS-IGF2)	ENSP00000348986.4:p.Ala98=
ENST00000397270.1:c.294C= (INS-IGF2)	ENSP00000380440.1:p.Ala98=
ENST00000476874.1:n.177C= (INS-IGF2)
ENST00000481781.1:n.499C= (INS-IGF2)
NM_001007139.5:c.-362C= (IGF2)	NP_001007140.2:n.-362C=
NM_001042376.2:c.294C= (INS-IGF2)	NP_001035835.1:p.Ala98=
NR_003512.3:n.353C= (INS-IGF2)
NM_001042376.3:c.294C= (INS-IGF2)	NP_001035835.1:p.Ala98=
NR_003512.4:n.353C= (INS-IGF2)
NM_001007139.6:c.-362C= (IGF2)	NP_001007140.2:n.-362C=