Canonical Allele Identifier: CA2611973761

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2149026-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149028del , CM000673.2:g.2149028del	GRCh38
NC_000011.9:g.2170258del , CM000673.1:g.2170258del	GRCh37
NC_000011.8:g.2126834del	NCBI36
NG_008849.1:g.5577del
NG_050578.1:g.17183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-249+99del (IGF2)	ENSP00000511998.1:n.-249+99del
ENST00000643349.2:c.254+99del	ENSP00000495715.1:n.254+99del
ENST00000695541.1:c.-249+99del (IGF2)	ENSP00000511997.1:n.-249+99del
ENST00000481781.2:n.345+99del
ENST00000643349.1:c.254+99del	ENSP00000495715.1:n.254+99del
ENST00000356578.8:c.407+99del (INS-IGF2)	ENSP00000348986.4:n.407+99del
ENST00000397270.1:c.407+99del (INS-IGF2)	ENSP00000380440.1:n.407+99del
ENST00000476874.1:n.389del (INS-IGF2)
ENST00000481781.1:n.612+99del (INS-IGF2)
NM_001007139.5:c.-249+99del (IGF2)	NP_001007140.2:n.-249+99del
NM_001042376.2:c.407+99del (INS-IGF2)	NP_001035835.1:n.407+99del
NR_003512.3:n.466+99del (INS-IGF2)
NM_001042376.3:c.407+99del (INS-IGF2)	NP_001035835.1:n.407+99del
NR_003512.4:n.466+99del (INS-IGF2)
NM_001007139.6:c.-249+99del (IGF2)	NP_001007140.2:n.-249+99del