Canonical Allele Identifier: CA2790177451

Gene: IGF2 INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148705T>C , CM000673.2:g.2148705T>C	GRCh38
NC_000011.9:g.2169935T>C , CM000673.1:g.2169935T>C	GRCh37
NC_000011.8:g.2126511T>C	NCBI36
NG_008849.1:g.5899A>G
NG_050578.1:g.17505A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-249+421A>G (IGF2)	ENSP00000511998.1:n.-249+421A>G
ENST00000643349.2:c.254+421A>G	ENSP00000495715.1:n.254+421A>G
ENST00000695541.1:c.-249+421A>G (IGF2)	ENSP00000511997.1:n.-249+421A>G
ENST00000481781.2:n.345+421A>G
ENST00000643349.1:c.254+421A>G	ENSP00000495715.1:n.254+421A>G
ENST00000356578.8:c.407+421A>G (INS-IGF2)	ENSP00000348986.4:n.407+421A>G
ENST00000397270.1:c.407+421A>G (INS-IGF2)	ENSP00000380440.1:n.407+421A>G
ENST00000481781.1:n.612+421A>G (INS-IGF2)
NM_001007139.5:c.-249+421A>G (IGF2)	NP_001007140.2:n.-249+421A>G
NM_001042376.2:c.407+421A>G (INS-IGF2)	NP_001035835.1:n.407+421A>G
NR_003512.3:n.466+421A>G (INS-IGF2)
NM_001042376.3:c.407+421A>G (INS-IGF2)	NP_001035835.1:n.407+421A>G
NR_003512.4:n.466+421A>G (INS-IGF2)
NM_001007139.6:c.-249+421A>G (IGF2)	NP_001007140.2:n.-249+421A>G