Canonical Allele Identifier: CA597431586

Gene: IGF2 INS-IGF2 IGF2-AS

Linked Data

• dbSNP Id: rs1485223688
• gnomAD v2: 11-2167623-C-CCT
• gnomAD v4: 11-2146393-C-CCT
• MyVariant Identifiers: chr11:g.2167623_2167624insCT (hg19) ; chr11:g.2146393_2146394insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2146395_2146396dup , CM000673.2:g.2146395_2146396dup	GRCh38
NC_000011.9:g.2167625_2167626dup , CM000673.1:g.2167625_2167626dup	GRCh37
NC_000011.8:g.2124201_2124202dup	NCBI36
NG_008849.1:g.8209_8210dup
NG_050578.1:g.19815_19816dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-7+1171_-7+1172dup (IGF2)	ENSP00000511998.1:n.-7+1171_-7+1172dup
ENST00000643349.2:c.*46+1171_*46+1172dup	ENSP00000495715.1:n.*46+1171_*46+1172dup
ENST00000695541.1:c.-7+1171_-7+1172dup (IGF2)	ENSP00000511997.1:n.-7+1171_-7+1172dup
ENST00000643349.1:c.*46+1171_*46+1172dup	ENSP00000495715.1:n.*46+1171_*46+1172dup
ENST00000356578.8:c.*46+1171_*46+1172dup (INS-IGF2)	ENSP00000348986.4:n.*46+1171_*46+1172dup
NM_001007139.5:c.-7+1171_-7+1172dup (IGF2)	NP_001007140.2:n.-7+1171_-7+1172dup
NR_003512.3:n.708+1171_708+1172dup (INS-IGF2)
NR_028043.2:n.587_588dup (IGF2-AS)
NR_133657.1:n.476_477dup (IGF2-AS)
NR_003512.4:n.708+1171_708+1172dup (INS-IGF2)
NM_001007139.6:c.-7+1171_-7+1172dup (IGF2)	NP_001007140.2:n.-7+1171_-7+1172dup