Canonical Allele Identifier: CA597431654

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs745902608
• gnomAD v2: 11-2170502-A-AG
• gnomAD v4: 11-2149272-A-AG
• MyVariant Identifiers: chr11:g.2170503_2170504insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149277dup , CM000673.2:g.2149277dup	GRCh38
NC_000011.9:g.2170507dup , CM000673.1:g.2170507dup	GRCh37
NC_000011.8:g.2127083dup	NCBI36
NG_008849.1:g.5331dup
NG_050578.1:g.16937dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-396dup (IGF2)	ENSP00000511998.1:n.-396dup
ENST00000643349.2:c.107dup	ENSP00000495715.1:p.Ala37CysfsTer7
ENST00000695541.1:c.-396dup (IGF2)	ENSP00000511997.1:n.-396dup
ENST00000481781.2:n.198dup
ENST00000643349.1:c.107dup	ENSP00000495715.1:p.Ala37CysfsTer7
ENST00000356578.8:c.260dup (INS-IGF2)	ENSP00000348986.4:p.Ala88CysfsTer7
ENST00000397270.1:c.260dup (INS-IGF2)	ENSP00000380440.1:p.Ala88CysfsTer7
ENST00000476874.1:n.143dup (INS-IGF2)
ENST00000481781.1:n.465dup (INS-IGF2)
NM_001007139.5:c.-396dup (IGF2)	NP_001007140.2:n.-396dup
NM_001042376.2:c.260dup (INS-IGF2)	NP_001035835.1:p.Ala88CysfsTer7
NR_003512.3:n.319dup (INS-IGF2)
NM_001042376.3:c.260dup (INS-IGF2)	NP_001035835.1:p.Ala88CysfsTer7
NR_003512.4:n.319dup (INS-IGF2)
NM_001007139.6:c.-396dup (IGF2)	NP_001007140.2:n.-396dup