Canonical Allele Identifier: CA2611973771

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2149029-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149029A>G , CM000673.2:g.2149029A>G	GRCh38
NC_000011.9:g.2170259A>G , CM000673.1:g.2170259A>G	GRCh37
NC_000011.8:g.2126835A>G	NCBI36
NG_008849.1:g.5575T>C
NG_050578.1:g.17181T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-249+97T>C (IGF2)	ENSP00000511998.1:n.-249+97T>C
ENST00000643349.2:c.254+97T>C	ENSP00000495715.1:n.254+97T>C
ENST00000695541.1:c.-249+97T>C (IGF2)	ENSP00000511997.1:n.-249+97T>C
ENST00000481781.2:n.345+97T>C
ENST00000643349.1:c.254+97T>C	ENSP00000495715.1:n.254+97T>C
ENST00000356578.8:c.407+97T>C (INS-IGF2)	ENSP00000348986.4:n.407+97T>C
ENST00000397270.1:c.407+97T>C (INS-IGF2)	ENSP00000380440.1:n.407+97T>C
ENST00000476874.1:n.387T>C (INS-IGF2)
ENST00000481781.1:n.612+97T>C (INS-IGF2)
NM_001007139.5:c.-249+97T>C (IGF2)	NP_001007140.2:n.-249+97T>C
NM_001042376.2:c.407+97T>C (INS-IGF2)	NP_001035835.1:n.407+97T>C
NR_003512.3:n.466+97T>C (INS-IGF2)
NM_001042376.3:c.407+97T>C (INS-IGF2)	NP_001035835.1:n.407+97T>C
NR_003512.4:n.466+97T>C (INS-IGF2)
NM_001007139.6:c.-249+97T>C (IGF2)	NP_001007140.2:n.-249+97T>C