Canonical Allele Identifier: CA216262032

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs573661046
• gnomAD v2: 11-2169955-G-GA
• gnomAD v3: 11-2148725-G-GA
• gnomAD v4: 11-2148725-G-GA
• MyVariant Identifiers: chr11:g.2169955_2169956insA (hg19) ; chr11:g.2148725_2148726insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148726dup , CM000673.2:g.2148726dup	GRCh38
NC_000011.9:g.2169956dup , CM000673.1:g.2169956dup	GRCh37
NC_000011.8:g.2126532dup	NCBI36
NG_008849.1:g.5878dup
NG_050578.1:g.17484dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000481781.3:c.-249+400dup (IGF2)	ENSP00000511998.1:n.-249+400dup
ENST00000643349.2:c.254+400dup	ENSP00000495715.1:n.254+400dup
ENST00000695541.1:c.-249+400dup (IGF2)	ENSP00000511997.1:n.-249+400dup
ENST00000481781.2:n.345+400dup
ENST00000643349.1:c.254+400dup	ENSP00000495715.1:n.254+400dup
ENST00000356578.8:c.407+400dup (INS-IGF2)	ENSP00000348986.4:n.407+400dup
ENST00000397270.1:c.407+400dup (INS-IGF2)	ENSP00000380440.1:n.407+400dup
ENST00000481781.1:n.612+400dup (INS-IGF2)
NM_001007139.5:c.-249+400dup (IGF2)	NP_001007140.2:n.-249+400dup
NM_001042376.2:c.407+400dup (INS-IGF2)	NP_001035835.1:n.407+400dup
NR_003512.3:n.466+400dup (INS-IGF2)
NM_001042376.3:c.407+400dup (INS-IGF2)	NP_001035835.1:n.407+400dup
NR_003512.4:n.466+400dup (INS-IGF2)
NM_001007139.6:c.-249+400dup (IGF2)	NP_001007140.2:n.-249+400dup