Canonical Allele Identifier: CA2611971181

Gene: IGF2 INS-IGF2 IGF2-AS

Linked Data

• gnomAD v4: 11-2148628-ATGGTGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148629_2148634del , CM000673.2:g.2148629_2148634del	GRCh38
NC_000011.9:g.2169859_2169864del , CM000673.1:g.2169859_2169864del	GRCh37
NC_000011.8:g.2126435_2126440del	NCBI36
NG_008849.1:g.5970_5975del
NG_050578.1:g.17576_17581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-249+492_-249+497del (IGF2)	ENSP00000511998.1:n.-249+492_-249+497del
ENST00000643349.2:c.254+492_254+497del	ENSP00000495715.1:n.254+492_254+497del
ENST00000695541.1:c.-249+492_-249+497del (IGF2)	ENSP00000511997.1:n.-249+492_-249+497del
ENST00000481781.2:n.345+492_345+497del
ENST00000643349.1:c.254+492_254+497del	ENSP00000495715.1:n.254+492_254+497del
ENST00000356578.8:c.407+492_407+497del (INS-IGF2)	ENSP00000348986.4:n.407+492_407+497del
ENST00000397270.1:c.407+492_407+497del (INS-IGF2)	ENSP00000380440.1:n.407+492_407+497del
ENST00000481781.1:n.612+492_612+497del (INS-IGF2)
NM_001007139.5:c.-249+492_-249+497del (IGF2)	NP_001007140.2:n.-249+492_-249+497del
NM_001042376.2:c.407+492_407+497del (INS-IGF2)	NP_001035835.1:n.407+492_407+497del
NR_003512.3:n.466+492_466+497del (INS-IGF2)
NR_028043.2:n.2031_2036del (IGF2-AS)
NR_133657.1:n.1920_1925del (IGF2-AS)
NM_001042376.3:c.407+492_407+497del (INS-IGF2)	NP_001035835.1:n.407+492_407+497del
NR_003512.4:n.466+492_466+497del (INS-IGF2)
NM_001007139.6:c.-249+492_-249+497del (IGF2)	NP_001007140.2:n.-249+492_-249+497del