Canonical Allele Identifier: CA1948016763

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs1860175225

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149307del , CM000673.2:g.2149307del	GRCh38
NC_000011.9:g.2170537del , CM000673.1:g.2170537del	GRCh37
NC_000011.8:g.2127113del	NCBI36
NG_008849.1:g.5298del
NG_050578.1:g.16904del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-429del (IGF2)	ENSP00000511998.1:n.-429del
ENST00000643349.2:c.74del	ENSP00000495715.1:p.Pro25GlnfsTer16
ENST00000695541.1:c.-429del (IGF2)	ENSP00000511997.1:n.-429del
ENST00000481781.2:n.165del
ENST00000643349.1:c.74del	ENSP00000495715.1:p.Pro25GlnfsTer16
ENST00000356578.8:c.227del (INS-IGF2)	ENSP00000348986.4:p.Pro76GlnfsTer16
ENST00000397270.1:c.227del (INS-IGF2)	ENSP00000380440.1:p.Pro76GlnfsTer16
ENST00000476874.1:n.110del (INS-IGF2)
ENST00000481781.1:n.432del (INS-IGF2)
NM_001007139.5:c.-429del (IGF2)	NP_001007140.2:n.-429del
NM_001042376.2:c.227del (INS-IGF2)	NP_001035835.1:p.Pro76GlnfsTer16
NR_003512.3:n.286del (INS-IGF2)
NM_001042376.3:c.227del (INS-IGF2)	NP_001035835.1:p.Pro76GlnfsTer16
NR_003512.4:n.286del (INS-IGF2)
NM_001007139.6:c.-429del (IGF2)	NP_001007140.2:n.-429del