Canonical Allele Identifier: CA2790177450

Gene: IGF2 INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148691_2148692del , CM000673.2:g.2148691_2148692del	GRCh38
NC_000011.9:g.2169921_2169922del , CM000673.1:g.2169921_2169922del	GRCh37
NC_000011.8:g.2126497_2126498del	NCBI36
NG_008849.1:g.5913_5914del
NG_050578.1:g.17519_17520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-249+435_-249+436del (IGF2)	ENSP00000511998.1:n.-249+435_-249+436del
ENST00000643349.2:c.254+435_254+436del	ENSP00000495715.1:n.254+435_254+436del
ENST00000695541.1:c.-249+435_-249+436del (IGF2)	ENSP00000511997.1:n.-249+435_-249+436del
ENST00000481781.2:n.345+435_345+436del
ENST00000643349.1:c.254+435_254+436del	ENSP00000495715.1:n.254+435_254+436del
ENST00000356578.8:c.407+435_407+436del (INS-IGF2)	ENSP00000348986.4:n.407+435_407+436del
ENST00000397270.1:c.407+435_407+436del (INS-IGF2)	ENSP00000380440.1:n.407+435_407+436del
ENST00000481781.1:n.612+435_612+436del (INS-IGF2)
NM_001007139.5:c.-249+435_-249+436del (IGF2)	NP_001007140.2:n.-249+435_-249+436del
NM_001042376.2:c.407+435_407+436del (INS-IGF2)	NP_001035835.1:n.407+435_407+436del
NR_003512.3:n.466+435_466+436del (INS-IGF2)
NM_001042376.3:c.407+435_407+436del (INS-IGF2)	NP_001035835.1:n.407+435_407+436del
NR_003512.4:n.466+435_466+436del (INS-IGF2)
NM_001007139.6:c.-249+435_-249+436del (IGF2)	NP_001007140.2:n.-249+435_-249+436del