Canonical Allele Identifier: CA2611971289

Gene: IGF2 INS-IGF2 IGF2-AS

Linked Data

• gnomAD v4: 11-2148639-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148639_2148640insC , CM000673.2:g.2148639_2148640insC	GRCh38
NC_000011.9:g.2169869_2169870insC , CM000673.1:g.2169869_2169870insC	GRCh37
NC_000011.8:g.2126445_2126446insC	NCBI36
NG_008849.1:g.5964_5965insG
NG_050578.1:g.17570_17571insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-249+486_-249+487insG (IGF2)	ENSP00000511998.1:n.-249+486_-249+487insG
ENST00000643349.2:c.254+486_254+487insG	ENSP00000495715.1:n.254+486_254+487insG
ENST00000695541.1:c.-249+486_-249+487insG (IGF2)	ENSP00000511997.1:n.-249+486_-249+487insG
ENST00000481781.2:n.345+486_345+487insG
ENST00000643349.1:c.254+486_254+487insG	ENSP00000495715.1:n.254+486_254+487insG
ENST00000356578.8:c.407+486_407+487insG (INS-IGF2)	ENSP00000348986.4:n.407+486_407+487insG
ENST00000397270.1:c.407+486_407+487insG (INS-IGF2)	ENSP00000380440.1:n.407+486_407+487insG
ENST00000481781.1:n.612+486_612+487insG (INS-IGF2)
NM_001007139.5:c.-249+486_-249+487insG (IGF2)	NP_001007140.2:n.-249+486_-249+487insG
NM_001042376.2:c.407+486_407+487insG (INS-IGF2)	NP_001035835.1:n.407+486_407+487insG
NR_003512.3:n.466+486_466+487insG (INS-IGF2)
NR_028043.2:n.2041_2042insC (IGF2-AS)
NR_133657.1:n.1930_1931insC (IGF2-AS)
NM_001042376.3:c.407+486_407+487insG (INS-IGF2)	NP_001035835.1:n.407+486_407+487insG
NR_003512.4:n.466+486_466+487insG (INS-IGF2)
NM_001007139.6:c.-249+486_-249+487insG (IGF2)	NP_001007140.2:n.-249+486_-249+487insG