Canonical Allele Identifier: CA2574752776

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2149404-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149404A>G , CM000673.2:g.2149404A>G	GRCh38
NC_000011.9:g.2170634A>G , CM000673.1:g.2170634A>G	GRCh37
NC_000011.8:g.2127210A>G	NCBI36
NG_008849.1:g.5200T>C
NG_050578.1:g.16806T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-468-59T>C (IGF2)	ENSP00000511998.1:n.-468-59T>C
ENST00000643349.2:c.-25T>C	ENSP00000495715.1:n.-25T>C
ENST00000695541.1:c.-468-59T>C (IGF2)	ENSP00000511997.1:n.-468-59T>C
ENST00000481781.2:n.126-59T>C
ENST00000643349.1:c.-25T>C	ENSP00000495715.1:n.-25T>C
ENST00000356578.8:c.188-59T>C (INS-IGF2)	ENSP00000348986.4:n.188-59T>C
ENST00000397270.1:c.188-59T>C (INS-IGF2)	ENSP00000380440.1:n.188-59T>C
ENST00000476874.1:n.71-59T>C (INS-IGF2)
ENST00000481781.1:n.393-59T>C (INS-IGF2)
NM_001007139.5:c.-527T>C (IGF2)	NP_001007140.2:n.-527T>C
NM_001042376.2:c.188-59T>C (INS-IGF2)	NP_001035835.1:n.188-59T>C
NR_003512.3:n.247-59T>C (INS-IGF2)
NM_001042376.3:c.188-59T>C (INS-IGF2)	NP_001035835.1:n.188-59T>C
NR_003512.4:n.247-59T>C (INS-IGF2)
NM_001007139.6:c.-527T>C (IGF2)	NP_001007140.2:n.-527T>C