Canonical Allele Identifier: CA216260350

Gene: IGF2 INS-IGF2 IGF2-AS

Linked Data

• dbSNP Id: rs370814727
• gnomAD v4: 11-2146266-T-TCCG
• MyVariant Identifiers: chr11:g.2167496_2167497insCCG (hg19) ; chr11:g.2146266_2146267insCCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2146270_2146272dup , CM000673.2:g.2146270_2146272dup	GRCh38
NC_000011.9:g.2167500_2167502dup , CM000673.1:g.2167500_2167502dup	GRCh37
NC_000011.8:g.2124076_2124078dup	NCBI36
NG_008849.1:g.8335_8337dup
NG_050578.1:g.19941_19943dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000481781.3:c.-7+1297_-7+1299dup (IGF2)	ENSP00000511998.1:n.-7+1297_-7+1299dup
ENST00000643349.2:c.*46+1297_*46+1299dup	ENSP00000495715.1:n.*46+1297_*46+1299dup
ENST00000695541.1:c.-7+1297_-7+1299dup (IGF2)	ENSP00000511997.1:n.-7+1297_-7+1299dup
ENST00000643349.1:c.*46+1297_*46+1299dup	ENSP00000495715.1:n.*46+1297_*46+1299dup
ENST00000356578.8:c.*46+1297_*46+1299dup (INS-IGF2)	ENSP00000348986.4:n.*46+1297_*46+1299dup
NM_001007139.5:c.-7+1297_-7+1299dup (IGF2)	NP_001007140.2:n.-7+1297_-7+1299dup
NR_003512.3:n.708+1297_708+1299dup (INS-IGF2)
NR_028043.2:n.462_464dup (IGF2-AS)
NR_133657.1:n.437-86_437-84dup (IGF2-AS)
NR_003512.4:n.708+1297_708+1299dup (INS-IGF2)
NM_001007139.6:c.-7+1297_-7+1299dup (IGF2)	NP_001007140.2:n.-7+1297_-7+1299dup