Canonical Allele Identifier: CA5817902

Gene: IGF2 INS-IGF2 IGF2-AS

Linked Data

• dbSNP Id: rs761566745
• ExAC: 11:2167499 G / GCCGTC
• gnomAD v2: 11-2167499-G-GCCGTC
• gnomAD v3: 11-2146269-G-GCCGTC
• gnomAD v4: 11-2146269-G-GCCGTC
• MyVariant Identifiers: chr11:g.2167499_2167500insCCGTC (hg19) ; chr11:g.2146269_2146270insCCGTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2146271_2146275dup , CM000673.2:g.2146271_2146275dup	GRCh38
NC_000011.9:g.2167501_2167505dup , CM000673.1:g.2167501_2167505dup	GRCh37
NC_000011.8:g.2124077_2124081dup	NCBI36
NG_008849.1:g.8330_8334dup
NG_050578.1:g.19936_19940dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000481781.3:c.-7+1292_-7+1296dup (IGF2)	ENSP00000511998.1:n.-7+1292_-7+1296dup
ENST00000643349.2:c.*46+1292_*46+1296dup	ENSP00000495715.1:n.*46+1292_*46+1296dup
ENST00000695541.1:c.-7+1292_-7+1296dup (IGF2)	ENSP00000511997.1:n.-7+1292_-7+1296dup
ENST00000643349.1:c.*46+1292_*46+1296dup	ENSP00000495715.1:n.*46+1292_*46+1296dup
ENST00000356578.8:c.*46+1292_*46+1296dup (INS-IGF2)	ENSP00000348986.4:n.*46+1292_*46+1296dup
NM_001007139.5:c.-7+1292_-7+1296dup (IGF2)	NP_001007140.2:n.-7+1292_-7+1296dup
NR_003512.3:n.708+1292_708+1296dup (INS-IGF2)
NR_028043.2:n.463_467dup (IGF2-AS)
NR_133657.1:n.437-85_437-81dup (IGF2-AS)
NR_003512.4:n.708+1292_708+1296dup (INS-IGF2)
NM_001007139.6:c.-7+1292_-7+1296dup (IGF2)	NP_001007140.2:n.-7+1292_-7+1296dup